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PCR Related Discussions
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to PCR the PCR product - (reply: 3)
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PCR product appear two close band in my gel! - (reply: 3)
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ITP substitutes... what? - can I add ITP to my degenerated primers to lower the degeneracy? (reply: 2)
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Multiplex pcr trouble - (reply: 4)
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no amplification in target gene - (reply: 1)
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need help...how to compare mouse vs human sequences for primer design - (reply: 2)
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Pfaffl Method... - Is there a range of acceptance for the PCR efficieny in Pfaffl method? (reply: 4)
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RT-PCR for small RNAs - (reply: 1)
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PCR problem (great different of Tm in primers) - (reply: 3)
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DNA PAGE - suitability of PCR buffer (reply: 1)
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Which DNA is good for PCR for amplify a certain sequence? cDNA or genomic DNA ? - (reply: 2)
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pcr amplification - right amplification,right sequence but still in dilemma (reply: 4)
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Amplification efficiency - (reply: 3)
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Create an artificial restriction site for a endonuclease and 53bp long primer? - (reply: 2)
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PCR sequencing/cloning-seq for SNP identification - (reply: 1)
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Tm of PCR primers: one 68, the other 58. Impossible to succeed? - (reply: 3)
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many bands on PCR products - is it unusual? (reply: 6)
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PCR product dimer - clean it up (reply: 3)
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single stranded binding protein? - how to put into my PCR reaction? (reply: 6)
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Primer design for PCR following ChIP - (reply: 3)
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Will salmon sperm DNA in ChIP protocol interfere the WGA amplification? - (reply: 1)
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PCR Inhibitor - Where/What are you? (reply: 9)
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How to name primers? - Any official nomenclature systems to name primers? (reply: 4)
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Primer dimers!? HELP - (reply: 8)
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PCR troubleshooting - (reply: 22)
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MSP primer does not work - (reply: 5)
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PCR PRINCIPLES SOS! - PCR (reply: 9)
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How to increase the product amount in BSP? - weak amplification in BSP (reply: 3)
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How primers can be measured? - (reply: 6)
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general PCR question - (reply: 15)
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RE sites on the primer. - How can I check for restriction sites on a primer sequence? (reply: 2)
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What are normalisation primers for the rt-PCR? - Im going to order the mirVana rt-PCR kit for miRNAs (reply: 1)
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DNA Extraction using Phenol and Ethanol - ETHANOL AND PCR (reply: 7)
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PCR product stuck in agaros wells - (reply: 8)
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RNA contamination in primers - (reply: 2)
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how 2 design rev.transPCR primer? - need functioning protocol.... (reply: 1)
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polyadenylation and RT-PCR - (reply: 2)
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methylnick.please help me with MSP primer designing! - (reply: 3)
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concentration of primers - (reply: 1)
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PCR efficiencies for analysis of relative real time data - (reply: 1)
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Can I still use PCR to select transfectatns - (reply: 1)
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End of PCR products destroyed - (reply: 2)
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RNA PCR - RNA PCR (reply: 4)
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Gene Expression level of apoptotic-related genes by qReal Time RT PCR - (reply: 1)
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About DAPK1 MSP primer design. - About MSP primer design. (reply: 4)
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Inverse PCR ligation - (reply: 1)
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PCR disappeared - there is no amplification (reply: 11)
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Primer design from mRNA or DNA - Confused about what sequence to use for design of GSP and pPCR primers (reply: 2)
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Oligoarray vs PCR Microarray - (reply: 2)
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deisgning primers with restriction site - (reply: 7)
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Questions about primer design for BSP in plant - shouldn't we take the mC in CHG CHH context into consideration? (reply: 3)
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RNA, cDNA, PCR - RT Inconsistency - High Quality RNA, Working RT, Varying PCR Results (reply: 2)
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RT-PCR works but not consistent - (reply: 3)
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cDNA primer help - (reply: 1)
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cDNA and primer Design Help - (reply: 6)
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Background amplification - (reply: 1)
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methylation specific PCR - (reply: 5)
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Bisulfite sequencing reproducibility - overlapping PCR amp primers give varying results (reply: 2)
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Making blunt ends DNA with T4 Polymerase - (reply: 6)
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Primer design program for Methylight - (reply: 3)
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PCR of ssDNA - (reply: 2)
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repeting PCR failing the reaction - (reply: 2)
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primer design software - primes for full lenth gene (reply: 3)
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mirVana™ qRT-PCR miRNA Detection versus miScript SYBR Green PCR kit - advantages and disadvantages (reply: 1)
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pcr amplification 5 kb - (reply: 4)
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PCR efficiency? - (reply: 3)
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Please help me design MSP primer! - (reply: 4)
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PCR fragment ligation - ligation of 3 pcr frangments (reply: 1)
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contmination PCR? - bands in - control but no bands in samples (reply: 2)
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What grade of primers for real-time TaqMan PCR assays? - (reply: 1)
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How much oligo dT cDNA to use in PCR - (reply: 3)
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Tm of the primers - company sends primers with lower Tm than expected (reply: 3)
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PCR problem - PCR did not work (reply: 5)
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PCR false positive reasons - (reply: 3)
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Is Klenow necessary for RT-PCR? - (reply: 3)
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PCR cycle - (reply: 1)
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ABI real time PCR instrument fail rate - Wondering whether we need the (expensive) service contract (reply: 5)
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RT-PCR primer design - RT-PCR primer design...need ur help (reply: 3)
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RT-PCR primer design - RT-PCR primer design...need ur help (reply: 1)
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Why am I only getting smears for my genomic DNA long-distance PCR products? - It worked great with sheep BACs but failed miserably for genomic DNA (reply: 4)
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PCR amplification - how to design the PCR program (reply: 4)
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PCR amplification - (reply: 2)
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PCR = products come randomly? - (reply: 4)
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primer sequence - reverse primer sequence (reply: 3)
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PCR cloning problem. Pls help...very urgent! - PCR cloning problem. Pls help...very urgent!!!!!!! (reply: 2)
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RT-PCR GAPDH Variability - (reply: 1)
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cDNA and additional bands when run on gel - I get a band o fthe same Mw regardless of the primers I use (reply: 2)
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PCR Optimization Question - Non-specific smearing around target level? (reply: 6)
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How far advance can you make PCR mix? - I'm a first time poster. (reply: 3)
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PCR troubleshooting - (reply: 10)
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signal amplification and facs - (reply: 1)
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pcr question - (reply: 5)
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Redundancy of real time PCR results - (reply: 2)
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PCR bands - why not straight ?&%#@&& - (reply: 3)
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Help with RT-PCR of 1.4Kb fragment - (reply: 2)
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how to optimize rt-pcr for gene expression analysis - (reply: 3)
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ghost band in PCR? - (reply: 11)
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PCR negative control contaminated and not the other wells - (reply: 4)
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What is my control when running a PCR reaction? - (reply: 2)
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RNA extraction for real time PCR from specific brain region - (reply: 1)
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How to synthesize your own oligo-dT primer - (reply: 4)
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PCR Problem - 300bp skip in the middle (reply: 9)
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A little more help with PCR! - (reply: 2)
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Designing Primers - (reply: 1)
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Basic question about setting up a PCR reaction - (reply: 4)
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Immunostaining - Amplification of signal - (reply: 1)
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basic basic question regarding pcr product storage - (reply: 2)
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rolling circle amplification - (reply: 1)
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mrna detection with sequence specific primers - (reply: 2)
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Normal PCR for looking expression - (reply: 1)
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Standard sequencing primers - how to find which sequencing primers bind to my DNA? (reply: 2)
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internal control primers for plants - (reply: 14)
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qRT-PCR primer design - (reply: 1)
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Where do you get your PCR primers from? - (reply: 3)
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Real Time PCR Efficiency - (reply: 3)
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genomic DNA contamination in RT-PCR - (reply: 7)
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PCR primers + large mRNA amplification - (reply: 5)
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how much cDNA do you use for RT-PCR? - (reply: 2)
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gDNA extraction from mouse ear for PCR - "Hot Shot" extraction (reply: 1)
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PCR WOES...... - STRATEGY DOUBT... (reply: 3)
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No PCR product visualized using quikchange kit - (reply: 10)
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Strange amplification pattern in DNA real time PCR - (reply: 4)
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PCR Primers for introducing tag - (reply: 5)
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Could have more DNA concentration inhibition effect on PCR? - (reply: 3)
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help design primer - (reply: 6)
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BLAST Help , Designing primers... - (reply: 5)
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help on PCR! - (reply: 2)
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pyrophosphate generation in PCR - (reply: 2)
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Different efficiency in different samples but the same primer - (reply: 1)
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housekeeping gene in klebsiella pneumoniae for RT PCR - (reply: 2)
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Long range PCR - (reply: 1)
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RT PCR of viral RNA segment - (reply: 1)
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Erroneous PCR product due to plasmid DNA contamination - (reply: 2)
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Primer design and degeneracy - Are synthesized sets identical? (reply: 2)
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Ghost contamination in Real Time PCR - (reply: 4)
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panomics promoter methylation PCR kit - results not what i expected (reply: 1)
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high fidelity PCR polymerase - ask for help! (reply: 3)
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primers amplify additional band (!) - (reply: 1)
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PCR Genotyping Problem - (reply: 7)
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resuspended primers in water - is this a problem?! (reply: 5)
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the mystery of the haunted pcr - Did my new preps degrade? Did my PCR fail? Or something more sinister? (reply: 5)
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Vent polymerase vs Klenow - (reply: 1)
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Do I need sterile RT-PCR tubes? - Real time PCR (reply: 5)
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Designing the primers for qRT PCR - Query - (reply: 14)
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doubts about melting curve, Ct... - understanding results from 1st real time PCR (reply: 5)
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primers sequence - (reply: 2)
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problem with WGA amplification of my chip sample - (reply: 4)
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Chip Troubles - Help: Strong PCR signal from negative control region (reply: 7)
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Image J for PCR analysis - File type (reply: 5)
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primer designing - (reply: 1)
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How to design PCR primer to amplify a very long sequence(about 9.7kb) - I want to amplify cDNA genome of HCV. It's about 9.7kb long (reply: 2)
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wierd rt-pcr - (reply: 1)
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how to check concentration of dNTP I bought - (reply: 3)
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genomic DNA PCR - is it the same as a cDNA PCR (reply: 9)
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Primer Design for nucleotide sequence - (reply: 1)
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spiking cDNA or PCR product for standanrd curve dilutions - (reply: 1)
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Primer dimer problem in MSP - (reply: 2)
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Unspecific PCR bands - Why that happens? (reply: 5)
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Attaching DNA bases - Creating primers and plasmids? (reply: 3)
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Primer doubts - (reply: 2)
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how to select a calibrator for relative gene expression in real-time PCR - also about the inconsistant about the triplicate of real-time PCR (reply: 6)
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PCR cloning - (reply: 5)
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PCR mixture - (reply: 2)
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Fast vs Standard PCR - (reply: 1)
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Why the addition of restriction sites to primers? - (reply: 3)
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RT-PCR to amplify ORFs - (reply: 3)
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Primer desing for transcript variant - (reply: 2)
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Transcript variation - measuring by RT-PCR - (reply: 3)
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Primer analysis sites - Any suggestions? (reply: 3)
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Problem with promoter PCR and cloning - (reply: 3)
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RAPD and viruses - RAPD using very very short primers (reply: 4)
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PCR components/DNA sample optimal amounts - ul of DNA and each component for a good reaction. (reply: 10)
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Long Range PCR - (reply: 8)
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please help me to be sure from design primer have it - (reply: 3)
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reverse-transcriptase PCR (internal control?) - (reply: 6)
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heparin in DNA - no working PCR (reply: 4)
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QIAquick PCR purification kit for in vitro transcription? - (reply: 6)
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when to set up a RT-PCR for mRNA expression? - detect transcription of transgene (reply: 1)
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LR PCR and running gels - Roche Expand Long Range dNTPack (reply: 5)
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When is the right time to adjust RNA concentrations for Rt-PCR? - (reply: 2)
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checking mRNA expression by reverse transcriptase PCR - (reply: 2)
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Panomics Promoter Methylation PCR Kit and Methylation specific Digests - (reply: 2)
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PCR for psoudomonas - (reply: 7)
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resuspend Primers in TE or in water? - (reply: 7)
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how to extract DNA from adenovirus for template of PCR - (reply: 2)
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ssr cross species amplification - (reply: 2)
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Colony PCR with Phusion - (reply: 7)
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Can we measure gene expression with standard PCR? - (reply: 1)
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manual primer desgining - (reply: 2)
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Abgene PCR master mix?-MgCl concentration - (reply: 1)
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DMSO in PCR - (reply: 4)
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Sybr Green real time pcr limit of detection - (reply: 1)
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single band -> multiple banding in PCR - (reply: 2)
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Taq polymerase expressing E. coli requested - (reply: 2)
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real-time PCR problem - (reply: 1)
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BLAST search of primer sequence - (reply: 3)
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newbie question on Primer design for MSP - (reply: 2)
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Best house keeping gene for RT-PCR - (reply: 6)
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Real-time PCR for mRNA stability - (reply: 2)
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RT-PCR inconsistant results - (reply: 1)
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How long can keep PCR product in room temperature? - somebody switched off PCR Machine (reply: 6)
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Oligo dT primer - oligo dT primer with non-T priming 3´ or with 5´ (reply: 3)
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gDNA template for PCR - (reply: 2)
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PRC reagents and equipments - Is a PCR machine robust? (reply: 2)
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annealing times in PCR - (reply: 6)
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Large smear in PCR - (reply: 2)
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Confirming published methylation primers - (reply: 1)
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developing real time PCR - (reply: 5)
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Help designing primers; also help with viewing GenBank - (reply: 3)
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false positives in PCR due to environmental contamination? - (reply: 7)
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I'm beginning PCR..... - (reply: 4)
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Primer design - How to - am a novice ? (reply: 6)
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PCR product size - (reply: 1)
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Primer optimization (with probes) - Urges... (reply: 2)
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Direct PCR from Gram positive bacteria - Is it possible? (reply: 3)
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arms PCR problem - (reply: 2)
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SNP - How to design the SNP primer (reply: 1)
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storing pcr samples - (reply: 19)
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Dilute your cDNA ? - for real time PCR (reply: 2)
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RT-PCR reagents KIT 1 or 2-step? - (reply: 3)
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amplifying small amounts of converted DNA or unconverted DNA? - (reply: 2)
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Extraction of PCR product from gel - (reply: 4)
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How to get GOOD rt-pcr bands - (reply: 7)
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Choice of one-step or two-steps RT-PCR - (reply: 3)
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PCR Puzzle- Unusal Bands - (reply: 13)
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Problems with Bisulfite PCR - (reply: 13)
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when does pcr products degrade like this? - images attached (reply: 7)
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Choosing Primer: random or Olig-dt ? - (reply: 2)
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problem in PCR pdt size - (reply: 4)
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how to synthesize the pcr primers - (reply: 3)
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designing degenerate primer - (reply: 2)
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Washing the spin columns from PCR purekit - (reply: 1)
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incorporation of restriction site in Primers - Help to design primer to clone gene in frame with fluorescent tag (reply: 2)
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Trouble inserting PCR derived insert into vector - Trouble inserting PCR derived insert into vector (reply: 2)
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how to design pcr primers - (reply: 7)
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RT-PCR primer design and in silico PCR - (reply: 4)
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PCR yield, can assess by absorbance without electroforesis? - (reply: 2)
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Checking mRNA expression by RT-PCR - (reply: 2)
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Primer extension and sequencing from total RNA - (reply: 1)
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primer design - over expression (reply: 1)
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RT-PCR no amplification - (reply: 2)
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Bisulfite PCR Question - (reply: 2)
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PCR bias with BSP primers - (reply: 1)
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quadraplex RT-PCR error - (reply: 1)
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final extension real time PCR - (reply: 4)
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cloning of a fluorecent PCR product - (reply: 1)
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pcr shelf life? - (reply: 1)
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NOT SyBrGreenPCR amplification in positive control-Why? - (reply: 1)
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Strange amplification curve - (reply: 2)
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how to improve PCR yield? - (reply: 5)
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PCR a fragment of 6kb - (reply: 14)
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TEST: embed video - PCR song - (reply: 4)
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Primer design and tolerances - (reply: 3)
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PCR to sequencing problems - (reply: 5)
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PCR Performance Test - QC test for new Taq Polymerase (reply: 3)
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EXOSAP-IT degrades my PCR products - (reply: 3)
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Internal Standards for RT-pCR - (reply: 11)
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Problems with amplification - (reply: 7)
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Can a 96 well plate for rt PCR be used for ELISA? - 96 well plate , ELISA (reply: 2)
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PCR master mix preparation - (reply: 11)
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primer design - (reply: 2)
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real time pcr newbie - (reply: 3)
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help with degenerate primer design - (reply: 1)
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PCR: Big Primers = Big Problems (for me) - I'm really not sure what's going on in those poor little tubes... (reply: 2)
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Questions about PCR amplification using cDNA (RT from total RNA). - (reply: 6)
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mutations in primer sequence - (reply: 2)
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How to get perfect amplification peaks - Share my long QPCR troubleshooting experience (reply: 1)
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Amount of DNA to run on gel - Be it from PCR or from DNA extraction steps (reply: 4)
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digestion of pcr - (reply: 2)
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Amplification Effeciency - solve the problem with E value (reply: 2)
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Recombinant PCR - (reply: 1)
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PCR Inhibition by DNA? - (reply: 5)
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pcr,ligation and transformation with RE SalI and XhoI - (reply: 4)
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RT-PCR from VERY limited quantity of tissue sample - Need suggestion on RNA isolation and RT kits to maximize cDNA yield (reply: 1)
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Nested primers - (reply: 5)
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Total RNA isolation for RT-PCR - (reply: 3)
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Primer design - Primer design for PCR with TE sites (reply: 2)
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Reverse transcriptation for qPCR with some specific primers. Should I use primer - (reply: 2)
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PCR and competent cells - (reply: 3)
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primer conditions for expression work - (reply: 5)
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DNA polymerase fidelity assay (NOT PCR-based) - (reply: 2)
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Failed RT-PCR amplification of 3-&5''-ligated small RNAs - (reply: 5)
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RT-PCR for various sample with Tm from 45-60 degree - (reply: 1)
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Question about primer design targeting GC-rich region - (reply: 2)
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promoter pcr using primers with restriction sites giving trouble - (reply: 7)
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how to optimize primer and cDNA concentration for real-time - (reply: 2)
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primer Question pVax1 RE / Kozak - (reply: 1)
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Help -designing primers for real time RT-PCR - (reply: 1)
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Is it possible to use a PCR cleaning kit to clean a band from a TAE-Agarose gel? - (reply: 1)
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getting long pcr from cDNA - (reply: 4)
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How many bases should be added to end of enzyme in PCR for effective cutting - (reply: 8)
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PCR from cDNA library - (reply: 1)
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help for long PCR product amplification - (reply: 4)
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clear culture, but PCR positive - (reply: 4)
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Primer design for SNP detection - (reply: 2)
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Bad primer efficiency during multiplex qPCR - (reply: 1)
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problems with low concentration DNA templates for PCR - (reply: 5)
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phophorylating PCR product after CIP - (reply: 2)
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re-pcr (2nd) different with pcr (1st) - (reply: 5)
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pcr template amount - (reply: 2)
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Inefficient RT-PCR, ¿bad cDNA? - don't know why (reply: 1)
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PCR with paraffin-embedded tissue DNA samples - I have had problems to amplify DNA samples from paraffin-embedded tiss (reply: 1)
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max primer length - 85 nt too long? - (reply: 5)
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Problems with amplification curve - (reply: 5)
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how to isolate ORF by PCR - (reply: 1)
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different transcription from 5' UTR than 3' UTR primers - (reply: 8)
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how to isolate gene through PCR - (reply: 3)
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recommended primers for caspase 8 & 9 - human (reply: 4)
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UBC primer PCR - (reply: 1)
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Optimising bisulphite PCR primers - (reply: 4)
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It is nessesary to apply aseptic technique for PCR? - (reply: 3)
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Strange large bands on my PCR gel, has anyone seen this before? - PCR (reply: 3)
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Primer design help - secondary structures - Please help me troubleshoot? (reply: 12)
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help with RT-PCR - DNase usage - (reply: 2)
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Help: Genomic DNA PCR - (reply: 3)
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PAGE with Realtime PCR product (Sybr Green) - Post-staining with ethidium bromide? (reply: 4)
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sequential PCR and purification before TA cloning - (reply: 1)
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PCR inhibition in FFPE DNA - (reply: 1)
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pcr template - (reply: 4)
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Determine specific primers and transgene copy number by PCR - (reply: 1)
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optimization of PCR conditions - to know that primers are specific and detect copy number (reply: 1)
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PCR with Betaine, DMSO, BSA, DTT - (reply: 5)
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Any Universal Primer for 3' of cDNAs of all mRNAs? - (reply: 2)
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A couple of (RT-PCR) cowboy questions - I feel the need, the need for speed (reply: 2)
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generating an array by gene amplification - (reply: 2)
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PCR on this gene - products always present? - (reply: 9)
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better primer for cDNA synthesis in real time pcr - (reply: 1)
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PCR cycle for 80 bases - (reply: 2)
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genome amplification before cloning? - (reply: 2)
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High concentration of antibiotics in amplification of plasmids - concerns about mutation of inserts in plasmid (reply: 1)
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can you judge a 22bp primer based on the 3' 10bp? - (reply: 6)
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my negative PCR control is still positive ! - (reply: 32)
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Is nested PCR always neccisary? - (reply: 3)
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Getting primer dimers in RT-PCR on and off? - (reply: 2)
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Internal control for RT-PCR analysis - The expression of internal control (reply: 3)
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PCR reaction - quick question! - (reply: 2)
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Quantitative PCR question - Comparative quant PCR with 16S rRna as reference gene (reply: 2)
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conc of cDNA to be used - PCR to test primers (reply: 5)
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What are different ways of genotyping a transgenic mouse? - what is best way to do genotyping--PCR, qRT-PCR or RT-PCR (reply: 3)
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optimum conditions for long pcr - (reply: 1)
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free programme for RT-PCR quantification - free programme for RT-PCR quantification (reply: 3)
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DIG pcr labeling and northern blot - (reply: 2)
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Primer for all HPV - (reply: 4)
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Weekly Decontamination Routine? - To prevent DNA contamination in a PCR lab (reply: 1)
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please help me check BSP primers. - (reply: 6)
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PCR on template with trinucleotide repeats - PCR tips for complexe DNA template (reply: 4)
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DNA PCR template - GC content (reply: 1)
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1:10 serial dilution in rt-pcr with slope of -0.58 ... - (reply: 1)
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using piece agarose band directly on PCR - does it work? - (reply: 3)
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Lengthy primers - (reply: 11)
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primer design - how far apart Tms could be? (reply: 4)
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positive colony PCR, but no insert!? - (reply: 5)
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Taq polymerase - (reply: 1)
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Steps in PCR - (reply: 1)
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PCR detection for latent infection of Human CMV - (reply: 1)
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ORF region amplification problem - (reply: 2)
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Free sample of GoTaq® Hot Start or any GoTaq® DNA Polymerase - (reply: 1)
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need help on microRNA real-time PCR - (reply: 6)
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Help for PCR - (reply: 1)
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PCR Help! - Primers-quality checking software (reply: 3)
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standard PCR efficiency - No real time! (reply: 2)
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design primers - (reply: 3)
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a problem about the Tm of the BSP primer - (reply: 2)
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DNA polymerase that produces blunt end and doesnt smear! - (reply: 2)
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Help! ignoring bad results in standard curve - about the pcr efficiency... (reply: 1)
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PCR on Genomic DNA from cell lysate - (reply: 5)
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PCR improvement - how to get more PCR product! (reply: 6)
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Primers distinguishing splicing alternatives - (reply: 1)
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Amplifying large gene - (reply: 2)
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Problem with bands of PCR products - (reply: 2)
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no more PCR amplification after I got rid of a contamination - (reply: 4)
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about PCR efficiency - (reply: 2)
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RT-PCR or disulfite treatment, which is better? - (reply: 5)
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TA cloning, sequencing results are vector self-ligation while bacterial PCR iden - (reply: 2)
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Sequencing result is vector self-ligation while bacterial PCR identification was - (reply: 5)
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primer design from mRNA - (reply: 12)
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who can give me a hand to check the BSP primer? - (reply: 5)
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How do you prevent PCR evaporation? - (reply: 9)
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Please help me design BSP primer. - (reply: 14)
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PCR contamination - (reply: 1)
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bisulfite PCR: is it my product? - (reply: 5)
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How can I create a T vector for PCR product cloning - (reply: 2)
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Should Taq polymerase be resuspended before use? - (reply: 3)
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PCR product won't come down from well - (reply: 3)
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Primer design: how do I add a restriction site to my primer? - (reply: 2)
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RE of PCR Fragment - (reply: 2)
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Gel purification of large plasmids for PCR or sequencing, HELP! - (reply: 3)
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Starting with semi quantitative RT-PCR and a little bit lost.. - (reply: 4)
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Help: PCR clone problem - (reply: 2)
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Storing primers...together? - (reply: 3)
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Genomic DNA fragment labeling by random priming - (reply: 1)
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different length for primers amplifying - (reply: 2)
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primer dilution - primer dilution from picomoles to micromolar (reply: 2)
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cytosolic PCR control - (reply: 1)
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PCR doesn´t work anymore - (reply: 3)
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Primer concentration is quantitative Real-time PCR - (reply: 1)
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Real time pcr in Rotor gene 6000- not getting positive results - (reply: 1)
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primer dimer annealing temperature - (reply: 2)
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design primers with custom end - To clone my gene into the MCS as fusions to the GFP tag (reply: 5)
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What is the function of acetate solution in DNA extraction for PCR used - (reply: 6)
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TetR primer - (reply: 1)
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choosing real-time PCR machine - (reply: 13)
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Sproadic PCR failures - (reply: 5)
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Sequencing:why do pcr AND cloning into plasmid? - (reply: 6)
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verify my microarray data - need help in real time PCR (reply: 1)
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some primer dilution calculations - (reply: 7)
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Band Intensity - Linear or Exponential? PCR Products - (reply: 4)
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PCR - reduced binding efficiency with lower Tm? - (reply: 2)
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Improving PCR specificity? - (reply: 2)
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Purified PCR product - (reply: 2)
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PCR product too short - (reply: 6)
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Housekeeping genes for RT-PCR in soybean - (reply: 6)
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primer tm with mismatch? - (reply: 6)
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cDNA quantification for PCR - (reply: 5)
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TOPO primer choice for sequencing - (reply: 3)
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no PCR product - (reply: 14)
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Real-Time PCR and Housekeeping gene - (reply: 9)
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Can do reverse transcription by gene-specific primers? - (reply: 3)
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Controls for real-time PCR... again - (reply: 7)
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Anchored oligo dT and Thermostable reverse transcriptase - temperature compatibility between RT and oligo dT priming (reply: 8)
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primer design with RE sites - (reply: 4)
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plz save my PCR product ! - (reply: 4)
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Transcript Amplification in genomic DNA PCR - (reply: 1)
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primer desighning with RE sites - (reply: 5)
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Taqman PCR master mix - (reply: 4)
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Primer design (long transcripts) - (reply: 2)
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PCR faint bands under UV light - (reply: 10)
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Primers for Real time PCR - Really need some advice (reply: 1)
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PCR Help - 2kbp product - (reply: 12)
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RNA amplification - (reply: 3)
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whole genomic amplification - (reply: 6)
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PCR product of unlinearized plasmid - (reply: 1)
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Stem-loop RT primers: how to anneal? - (reply: 1)
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help!real-time PCR to see gene's expression after treatment with cytokin - (reply: 4)
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second strand cDNA synth without primer? - (reply: 2)
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do you put two pairs primers in one tube when you do site mutations? - (reply: 2)
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General question about restriction sequences in PCR primers - (reply: 3)
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Will TOPO TA cloning work on "old" purified PCR product? - (reply: 4)
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SYbrgreen PCR protocol for the rookie - (reply: 1)
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Can PCR on same sample give different results when repeated? - (reply: 2)
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GAPDH primer sequence - cloning of huGAPDH gene (reply: 2)
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RT PCR for methylation analysis - (reply: 3)
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After detect PCR cannot get any colony with right direction of insert - insert direction (reply: 2)
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RT-PCR cloning: oligo dT-primed cDNA synthesis or anchored? - (reply: 1)
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Induction by IPTG of T7-RNA polymerase in BL21 strains : time lag? - (reply: 2)
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chip assay primers - chip assay primers (reply: 2)
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Genotyping PCR - (reply: 3)
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suitable length DNA for PCR? - (reply: 2)
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Setting up and analysing real time PCR - (reply: 2)
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how to add bases to the primer restriction sites - (reply: 2)
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PCR inespecific band amplification - (reply: 2)
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Problems with making mix of PCR reagents ? - (reply: 4)
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Questions about Stratagene QickChange Multi-mutagenesis - about how many primers and template DNA size (reply: 5)
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primer design - (reply: 3)
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PCR - Anomalous mobility of PCR product (reply: 2)
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SYBR green PCR - (reply: 4)
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Melting curve - SYBR Green PCR (reply: 8)
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PCR problem, no amplicon, tried everything I could think of.. - (reply: 6)
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Anyone know how can I precipitate PCR product in 96-well plate? - (reply: 2)
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How to ressuspend primers for Sybr? - (reply: 3)
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Ligation problem with PCR product cloning - (reply: 9)
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simple primer calculation - (reply: 5)
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WGA problems CpG island amplification - (reply: 6)
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What's wrong with my pcr? - high temperture with low specificity (reply: 6)
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PCR cloning-primer design and ligation - (reply: 20)
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RT-PCR Vs qRT-PCR help please! - (reply: 4)
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picking primers - (reply: 4)
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300 bp more after PCR purification - please help - (reply: 3)
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16s primers and PCR - (reply: 1)
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primer/probe mix for standard generation? - (reply: 2)
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Primers from RT-PCR database - RT-PCRdatabase primers giving primer dimers (reply: 1)
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Fast way to get plasmid for PCR - (reply: 2)
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restriction enzyme site with primers - (reply: 4)
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PCR efficiency for qRT-PCR analysis - PCR efficiency for qRT-PCR analysis (reply: 4)
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PCR product cloning - (reply: 6)
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PCR failure. GC problem? - (reply: 7)
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minimum mRNA concentration for RT-PCR - (reply: 4)
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Help. Trying to sequence my plasmids, but the primers refuse to prime! - (reply: 1)
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weird problem with Primers! - problem with the gene sequence i used to design my primers (reply: 4)
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Degnerate PCR and Sequencing Reactions - (reply: 4)
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pcr issue-gene not amping - (reply: 3)
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Forward n reversre primer Tm difference is 10 degree - (reply: 1)
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Primer mismatch bother me! - when enzyme sites added at 5' ends, mismatch increases. (reply: 1)
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Smearing in PCR - (reply: 4)
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Troubleshooting RT-PCR - (reply: 7)
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Why using heated-top or add mineral oil in PCR - (reply: 2)
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do I get right PCR product - (reply: 20)
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primer design (downloadable) programs - not online tools (reply: 4)
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yeast colony PCR - How to improve yeast colony PCR (reply: 7)
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BLOOD storage and PCR problems! HELP - (reply: 1)
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pcr problems - pcr to solve (reply: 2)
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PCR water contamination - (reply: 5)
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Thermostable Reverse Transcriptase for RT-PCR - (reply: 3)
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figure out the size of amplicon using known primer - (reply: 3)
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real time PCR data analysis - method I have never heard of before (reply: 3)
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Primer concentration... - (reply: 5)
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microgram per microlitre primer to molarity conversion.. - calculation plss (reply: 1)
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How to amplify PCR product - wonder why using linear fragment as template, PCR result was always sm (reply: 1)
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Can I run q RT real-time PCR based on cDNA amount? - (reply: 1)
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Long PCR primers for epitope tagging - where to order? (reply: 3)
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PCR screening for recombinant clones - (reply: 1)
-
Extremely Low Yield PCR with restriction site addition - Assistance requested for beginning molecular biologist on PCR techniqu (reply: 3)
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***MSP Primer Troubleshooting Specificity*** - (reply: 6)
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Problems amplifying unstable construct in E.coli - Tips needed (reply: 2)
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false positive in colony screening PCR? - (reply: 8)
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RT-PCR consistency - (reply: 2)
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No PCR product with verified primers on templates - Where is the bug???? (reply: 2)
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dried out pcr product - (reply: 1)
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Problem with amplifying bisulfite treated DNA from FFPE tissue - (reply: 3)
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Please see the PCR electropherogram - What's wrong with my pcr? (reply: 8)
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How good are my PCR primers? can I go with it?! - (reply: 2)
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PCR inhibitors - help ??!! (reply: 8)
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Bands in Negative control PCR - (reply: 18)
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QPCR primer Pairs - (reply: 1)
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primer design for unknown cDNA sequence - (reply: 1)
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Random Amplification + TA cloning = HATE - (reply: 2)
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touchdown qPCR - using degenerative primers (reply: 2)
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Quikchange PCR dNTP mix? - (reply: 8)
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primer Tm for PCR mutagenesis - (reply: 1)
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Inconsistent bisulfite PCR - (reply: 8)
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Restricition enzyme qouted in paper doesnot cut the PCR product according to the - (reply: 3)
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ISH vs. Real Time PCR - correlation between CT-values and quantity - (reply: 2)
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96 WELL PCR Purification Suggestions - (reply: 4)
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no PCR product! any advice? - (reply: 14)
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Identification of monomers/dimers in whole cell lysate via SDS-PAGE - (reply: 3)
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New to rt pcr real time - guidelines and advice (reply: 3)
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what to do when Tm > annealing temperature for PCR - (reply: 8)
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overlap extension pcr - (reply: 1)
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Polymerase for Quikchange mutagenesis - (reply: 3)
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Quikchange mutagenesis primer and PCR design - (reply: 3)
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Primer design - Issues with GAPDH primer blast search (reply: 2)
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PCR inhibitors in soil DNA - (reply: 6)
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primers dont match FASTA gene sequence... 'm confused - (reply: 11)
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How to know tissue specific gene expression by real time PCR - (reply: 3)
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sequence retrieval for primer design - (reply: 2)
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Statistics: real-time RT-PCR - (reply: 4)
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RT-PCR using formaldehyde cross linked samples - RNA extraction using CHIP crosslinked samples (reply: 1)
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PCR of AT-rich DNA - (reply: 3)
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phantom non specific amplification at high ct values - (reply: 7)
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Primer conc - (reply: 6)
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cDNA cloning using Taq/pfu polymerase - (reply: 2)
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Non-specific Real time PCR signals - (reply: 1)
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Mutagenesis PCR transforming into BL21(DE3) - (reply: 2)
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Does anyone know how to design LUX primers - (reply: 2)
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PCR amplificaiton isnt working - (reply: 12)
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Problems on overlap extenstion PCR - (reply: 2)
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A-overhang in PCR product - (reply: 2)
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Cox-2 primer for PCR - method how to search good cDNA in Pubmed (reply: 1)
-
How to purify 700bp pcr product? - (reply: 5)
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ChIP PCR problems - I can't get rid of the smears! - (reply: 6)
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why my pcr failed? - (reply: 5)
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PCR primers for CRISPR - primer3 isn't helpful in this case (reply: 1)
-
primer design for subclone - (reply: 2)
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QPCR versus regular PCR for Chip - (reply: 2)
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Could you run Taqman PCR on gel to see the band? - (reply: 1)
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Is it necessary to measure the amount of DNA before PCR? - (reply: 3)
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Polymerase - (reply: 3)
-
miRNA real time PCR - miRNA real time PCR (reply: 2)
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Mutagenesis and primer purity? - (reply: 4)
-
DNA amplification for chip-on-chip - WGA or LM-PCR or others? (reply: 12)
-
Trouble-shooting PCR with Origene vectors - I cannot get PCR to work, and I have tried many approaches (reply: 11)
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PCR primer design, real time versus old school - (reply: 2)
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Faint Band - PCR reaction - (reply: 2)
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Assembly PCR problem - (reply: 3)
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PCR TROUPLESHOOTING - (reply: 3)
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Amplifying cultures - quick question - (reply: 3)
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Real TIme PCR problems - (reply: 2)
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I have a problem with the M13 tailed primer method - M13 tailed primers-SSR (plants) (reply: 1)
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Fusion PCR problem: smear! - (reply: 3)
-
PCR Tubes - what kind of lid ? (reply: 6)
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problem with unspecific PCR product - (reply: 3)
-
What in ChIP samples inhibit PCR? - (reply: 2)
-
PCR variability or bad cell source? - (reply: 1)
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Storage of a plate for real time PCR - Ever stored your already prepared plate for real time PCR? (reply: 7)
-
RNA polymerase II antibody recommendation? - (reply: 2)
-
specific PCR polymerase - (reply: 3)
-
RT-Pcr without RNA isolation? - (reply: 3)
-
help with site-directed mutagenesis - What polymerase and cells to use? (reply: 3)
-
PCR to produce 1.6kbp insert in fragments - (reply: 5)
-
MULTIPLEX REAL-TIME PCR WITH SYBR-GREEN - (reply: 1)
-
RT PCR Standard curve amplification problem - (reply: 1)
-
cloning 708bp PCR prodyct into pET101 vector (TOPO) - (reply: 2)
-
Pfu + Taq polymerase and poly-A tails - (reply: 8)
-
Primer3 results - (reply: 2)
-
Help for Real-time PCR equipment choice - (reply: 4)
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Problems with several unspecific bands after PCR - (reply: 2)
-
PCR purification /DMSO / vanishing DNA - (reply: 2)
-
Colony PCr - (reply: 4)
-
PCR contamination - (reply: 9)
-
Cloning PCR product blunt + restriction site - (reply: 2)
-
help in cloning 6kb pcr fragment into topo? - (reply: 5)
-
cDNA synthesis using random hexamer vs. oligo dt primers - (reply: 2)
-
PCR of lambda phage - (reply: 1)
-
real time pcr with RNA co-precipitated with glycogen - (reply: 3)
-
Checking Insert using PCR from plasmid DNA? - (reply: 4)
-
transfect from full plasmid and transfect from PCR product - (reply: 5)
-
Problems with TA cloning of bisulfite converted PCR product - (reply: 2)
-
PCR problem..... - (reply: 4)
-
urgent help-how to get amplification from very low target copy number and how to - "Taqman probe" qPCR and "rotor gene 6000" machine (reply: 4)
-
PCR primers with overhangs - (reply: 2)
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pcr contamination - (reply: 4)
-
How to reduce the dimers - (reply: 3)
-
Digest-Ligase-PCR Problems (T-DNA fingerprinting gone wrong) - After ligating digested product and doing PCR on it i get no DNA smear (reply: 2)
-
magnesium concentration in pcr - (reply: 4)
-
Unspecific PCR problem - (reply: 2)
-
Primer designing - (reply: 1)
-
Designation of PCR primers in ChIP experiment - (reply: 3)
-
What is your favorite tool for primer design ? - (reply: 2)
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Routine PCR isn't working - (reply: 3)
-
Primer express? - Do you use it? (reply: 2)
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Bad primer design ? How can I know ? - How could I know if a primer would recognize a particular sequence ? (reply: 2)
-
The best reverse transcriptase for RT PCR - (reply: 5)
-
What is the proper upper limit of false priming in real time? - (reply: 3)
-
Ooops, forgot to add Mg to PCR! - But samples amplified! Can I use them? (reply: 3)
-
ancient DNa and PCR - (reply: 1)
-
Genotyping - Primers for PCR genotyping (reply: 5)
-
Real TIme PCR problems - (reply: 3)
-
Enzyme sites on Primer - (reply: 3)
-
PCR to identify Ig heavy chains (as a diagnostic for immune response) - (reply: 4)
-
PCR troubleshooting - (reply: 1)
-
PCR of mitochondrial fraction of nuclear-coded mitochondrial proteins - (reply: 4)
-
gene-specific Primer for qRT-PCR - (reply: 2)
-
BSA in PCR reaction - (reply: 1)
-
how to explain this strange amplification chart? - the Ct value comes to be very low because of the unusual amplification (reply: 1)
-
Designing RT-RCR Primers according to other species' homology - Using conserved regions as a guide when mRNA isn't known in your a (reply: 1)
-
PCR Troubleshooting - (reply: 2)
-
Nested PCR - (reply: 5)
-
No signal in Real-time but in normal PCR?! - (reply: 2)
-
primer design for PCR cloning - (reply: 1)
-
What is the suitable product size for conventional RT-PCR analysis - products with size over 1 kb? (reply: 6)
-
gDNA contamination in realtime PCR - (reply: 4)
-
deletion PCR? - I need help (reply: 1)
-
your experience with long range PCR - (reply: 3)
-
need help to evaluate primer sets for SYBR green qPCR - (reply: 2)
-
Real-time PCR low efficiency - (reply: 1)
-
PCR troubles - PCR works one day but not the next (reply: 10)
-
pcr product purification - (reply: 7)
-
PCR from cell culture - to detect the presence of adenovirus (reply: 2)
-
PCR mix for genotyping - (reply: 1)
-
Wrong PCR product after Bisulfite Treatment-reason? - (reply: 1)
-
DNA yields with the Qiagen PCR gel purification kit - (reply: 8)
-
PCR smear with CHIP - (reply: 2)
-
cassette pcr - (reply: 2)
-
Smear in PCR after ChIP - (reply: 2)
-
I need an animation of a PCR reaction - (reply: 4)
-
What happens if different templates dilution in Real-time PCR reaction - (reply: 1)
-
colony PCR screening, drove my crazy! need ur suggestion - (reply: 2)
-
PCR amplification of region with many ATT repeats - (reply: 1)
-
Unable to ligate two PCR products - (reply: 4)
-
PCR primers artifact - (reply: 2)
-
Purification of digested PCR product (a smear fr 200bp to 3kb) - (reply: 1)
-
weak RT-PCR product - (reply: 2)
-
qPCR primer efficiancy - (reply: 2)
-
How many cycles in PCR would you recommend for ChIP - (reply: 3)
-
Primer Express by ABI - (reply: 2)
-
real time PCR template - template concentration (reply: 3)
-
High Ct Values, low amplification - (reply: 3)
-
primer design for site-directed mutagenesis - (reply: 3)
-
using nanodrop to measure PCR product - (reply: 3)
-
what affects primer specificity? - (reply: 2)
-
Assembly PCR - Design of PCR program for primers w/low Tm? (reply: 2)
-
modification of PCR buffers - When and how (reply: 1)
-
Templiphi amplification kit: How to determine the amount of DNA product - (reply: 2)
-
how to switch to a gene in a vector using PCR or restriction enzymes? - gene is in pIVS2 vector (reply: 3)
-
Primers PCR - storage (reply: 5)
-
Dealing with VERY Mg sensitive PCR reactions - (reply: 4)
-
MSP: M and U primers products - (reply: 1)
-
Verifying Restriction sites generated in PCR of insert for subcloning - No colonies in transformation!Ligation issues?Insert issue? (reply: 4)
-
Multiple bands in PCR - (reply: 6)
-
Can I use different amount of cDNA template to run real time PCR? - when the amount of templates are different,Can I use reference gene to (reply: 2)
-
PCR from genomic DNA - (reply: 3)
-
Human Epigenome Project primers? - (reply: 2)
-
Creating short dsDNA from primers for cloning - (reply: 2)
-
Degenerate Primers - Help with Degenerate Primers (reply: 1)
-
RNA polymerase a sa fractionation control? - (reply: 3)
-
PCR screening of colonies - (reply: 3)
-
problems with mutant PCR - problems with mutant PCR (reply: 1)
-
Colony PCR running as smears - (reply: 1)
-
Trouble with doing DNA Isolation and then running a PCR - (reply: 6)
-
PCR: Can you get amplification if only one primer anneals? - Same size pcr product using 2 different primer sets (reply: 8)
-
10 fold dilutions show no RT-PCR product whatsoever - (reply: 1)
-
RT-PCR - necessary to run electrophoresis gels? - (reply: 4)
-
RNA handling for RT-PCR? - (reply: 4)
-
PCR cloning: neg self-ligation control, many colonies but no insert - (reply: 3)
-
phage cDNA library screening with PCR - (reply: 3)
-
PCR help! - urgent (reply: 5)
-
PCR trouble: about the annealing temperature - (reply: 4)
-
ready to use primers for BSP - (reply: 4)
-
PCR PROTOCOL FOR A BEGINNER - (reply: 11)
-
Troubles in PCR the converted DNA in promoter region - (reply: 6)
-
taqman is giving initially raised then fall off amplification curve why? - changed template concentraion n baseline too.....but ? (reply: 2)
-
Are there any special rules for primer design? - (reply: 5)
-
what's the difference between sequencing primer and cloning one. - confused (reply: 5)
-
ELISA in a real-time PCR plate - possible? (reply: 3)
-
sequencing issue - Internal primers (reply: 9)
-
GAPDH primer sequences for mRNA level in HeLa cells - (reply: 2)
-
RT PCR Primer dimer tissue dependent SYBR - (reply: 1)
-
Unnatural smear in PCR product - (reply: 7)
-
Can we compare traditional RT-PCR results with Real Time RT-PCR? - (reply: 1)
-
ChIP PCR help, maybe is the problem of SDS. - (reply: 4)
-
FGF20 PRIMER - (reply: 2)
-
Colony PCR - (reply: 8)
-
normality distribution in data - real-time PCR (reply: 2)
-
how to check normal distribution of data - real-time PCR data (reply: 2)
-
Cleaning up PCR products for BSP - Any experience with ExosapIt? (reply: 5)
-
Insert PCR - (reply: 1)
-
qPCR for microRNAs - minimal primer length? (reply: 6)
-
mutant PCR - (reply: 4)
-
Ligation of purified PCR product to Topo plasmid (with T7 promoter) and Transfor - (reply: 2)
-
DNA purification technique - After a PCR (reply: 8)
-
plant genomic DNA isolation and PCR - does CTAB affect PCR ? (reply: 4)
-
primer design for Syber Green - (reply: 1)
-
primer sets to do pyrosequencing - (reply: 3)
-
DGGE - PCR and gel conditions - (reply: 2)
-
not reproducible : reverse - transcription PCR - (reply: 5)
-
PCR machine choice: - (reply: 14)
-
primer walking design tool - (reply: 1)
-
PCR OF HIV genome - (reply: 1)
-
Agarose gel concentration for small and similar pcr pdts - (reply: 7)
-
Cloning a 60 bp pcr product and Mixing Pfx and Taq polymerases - (reply: 4)
-
PCR cloning problems - argh!!! (reply: 5)
-
optimizing PCR for low Tm primers - (reply: 1)
-
primer design for MSP and BSP - primers must be in promoter region? (reply: 1)
-
Minimal nucleotide for Taq polymerase binding - (reply: 1)
-
PCR efficiencies calculation - (reply: 2)
-
primers TM - (reply: 8)
-
do you subtract gel base intensity from PCR band intensity? - urgent require (reply: 3)
-
pcr product degradation - (reply: 1)
-
any problems with RT-PCR for large amplicon sizes? - very strange amplification curves (reply: 2)
-
Colony PCR - (reply: 11)
-
Degenerate Primers and dI - (reply: 5)
-
primer dissolved in wrong buffer (1M Tris HCl) - what to do now?? (reply: 7)
-
pcr mutagenesis - (reply: 4)
-
designing a primer - (reply: 5)
-
preference for region of primer design for qRT-PCR - (reply: 1)
-
using primers programms - (reply: 9)
-
problem rt pcr long gene - (reply: 4)
-
qPCR housekeepers - primers or probes? - (reply: 1)
-
gDNA PCR - for promoter amplification (reply: 1)
-
pcr for gene fusion - (reply: 3)
-
PCR Trouble Shooting - new primer, wrong dilution of primers, wrong band, and many more (reply: 15)
-
basic question regarding PCR - (reply: 7)
-
Ligation of pBBR with PCR fragments doesn't work - (reply: 3)
-
freaky primers - (reply: 5)
-
long range PCR primer design - (reply: 1)
-
How do you design primers of PCR-STR used in Forensic Medicine - Urgent!!!! (reply: 2)
-
Long Range PCR - (reply: 3)
-
what is CDS primer used as a control for QPCR in CHIP? - (reply: 2)
-
Primer tag info - (reply: 1)
-
How to get rid of primer dimers - (reply: 2)
-
Free sample from Takara. - All kind of polymerase for PCR and real-time PCR. (reply: 7)
-
problems with PCR primers - (reply: 15)
-
PCR of pBluescript unknown insert - (reply: 1)
-
one nucleotide in the primer is wrong - (reply: 2)
-
Primer Dilution. ...water or buffer? - (reply: 15)
-
How PCR product becomes gelly? - (reply: 1)
-
Nested PCR for BSP question - (reply: 4)
-
Flag Tagging a PCR product - (reply: 2)
-
What is the Ct standard deviation for the same sample in the whole pcr plate? - (reply: 2)
-
genomic DNA extraction - for PCR (reply: 1)
-
RANDOM PCR PROTOCOL? - Looking but no finding... (reply: 1)
-
PCR thermocycler (Eppendorf) - noise problem (reply: 1)
-
has any guys here had experience with poly(A) polymerase - (reply: 1)
-
real time pcr in a day - (reply: 5)
-
Help me for DNA concentration for PCR - (reply: 4)
-
PCR efficiency - (reply: 2)
-
PCR and Digest cleanup before ligation. - A shortcut by avoiding gel purification. (reply: 15)
-
Triton X in PCR - (reply: 7)
-
PCR unspecific amplification - (reply: 10)
-
real time PCR using two sets of primers with different melt curves - (reply: 4)
-
Overcoming PCR bias before bisulfite sequencing?! - (reply: 2)
-
AmpliTaq Gold - high fidelity polymerase? - (reply: 2)
-
What type of PCR to identify a plasmid insert? - (reply: 4)
-
Protocol for amplification of gene in plasmid directly from transformed e. coli? - (reply: 2)
-
problem in getting results from a optimized PCR - (reply: 5)
-
real-time PCR products on gel look good but melting curve is horribel - (reply: 2)
-
Howto: Maximum possible yield from a PCR? - What to optimize: Mgcl/primers/Polymerase/enhancers? (reply: 4)
-
Introduce restriction sites with PCR primers - (reply: 2)
-
Real-time PCR optimization - (reply: 8)
-
How much DNA in PCR? - (reply: 6)
-
Different sequencing result of PCR products from the same cDNA - (reply: 2)
-
Free FastStart Universal Real-Time PCR Master Mixes from Roche - (reply: 7)
-
PCR problems when amplifying sequence from gDNA - amplification of ~1.2 kb from gDNA (reply: 7)
-
primer flaw I'm missing? - (reply: 7)
-
MSP Primer design -rules to choose primers and reasons - (reply: 2)
-
Blunt end cloning PCR product - (reply: 6)
-
PCR problems - Fungal DNA (reply: 6)
-
PCR contamination that comes and goes! - (reply: 5)
-
gel purification for PCR product - (reply: 5)
-
How long we can keep Diluted Primer? - (reply: 5)
-
Primer calculation - (reply: 3)
-
Real-time PCR....Making sense of it all? - (reply: 3)
-
Real-time PCR vs. Northern Blotting / mRNA stability assays... - Advice from those who have experience with mRNA stability assays, plea (reply: 2)
-
PCR primer resuspend method? - (reply: 9)
-
Testing newly designed primers prior to real time - (reply: 2)
-
Getting rid of RNA & RNAse contamination in DNA sample for PCR - (reply: 8)
-
autoclave PCR tubes... - (reply: 8)
-
RT PCR produces nice crisp band but of wrong length :-) - (reply: 2)
-
multiple displacement amplification - (reply: 2)
-
Help needed. PCR band problem - (reply: 4)
-
PCR 'contamination' - (reply: 16)
-
2/3Kb PCR fragment - 16S/23S (reply: 3)
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About Degeneracy of a degenerate primer~~ - (reply: 2)
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Where do dNTP come from? - Chemical or Biological? (reply: 12)
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strange red lines in all of my agarose gels from PCR - (reply: 2)
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polimorph markers in inbred mouse strains? - microsatellites or any PCR based suggestins are wellcome! (reply: 1)
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PCR on PCR product - (reply: 5)
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RT-PCR gene specific amplification problem - (reply: 1)
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Cloning short sequences - Does PCR can help clones upto 70 bps into a protein sequence (reply: 10)
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information regarding PCR using very long primers - (reply: 4)
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RT-PCR: Band in no reverse transcriptase lane - (reply: 18)
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Non repeatability of RT-PCR with same cDNA - (reply: 3)
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what is the plasmid nomenclature: eg.what does it mean by pUC, pCR, and other ve - (reply: 13)
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MSP primer design - understanding the basics - (reply: 2)
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How get GFP signal without mRNA target from pIRES-EGFP - positive by FACS but no DNA amplifation from RT-PCR (reply: 8)
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Bisulfite: PCR condition or primer problem? - (reply: 13)
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Real-time PCR to analyze DNA methylation - (reply: 3)
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I really need an answer on PCR (16s rRNA), PLS PLS PLS! - (reply: 2)
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Primer concentration and standard curve slope in "Relative Standard Curve M - (reply: 1)
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storage of primers - (reply: 3)
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real time pcr designing software - (reply: 1)
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Problem with pcr, help required - PCR product (reply: 12)
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smearing in PCR product - (reply: 4)
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Curious - different primer synthesis? - (reply: 4)
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2-step RT-PCR - (reply: 1)
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Windows in PCR/Clean rooms..... - (reply: 8)
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'ladder bands' in PCR - (reply: 11)
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help a student with a PCR process question? - (reply: 6)
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Polymerase for Long PCR - (reply: 5)
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too many hits on Blast for primers / microsatellite - (reply: 4)
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Sequencing PCR products with biotin-labelled primer - (reply: 1)
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sequencing new "unknown" plasmid - any good SV40 primers out there? (reply: 1)
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"Ligate" two overlapping pcr products with PCR fusion? - (reply: 1)
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how to get DNA sequences starting from the primer - (reply: 4)
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Primer orientation, forward and reverse - (reply: 4)
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How to remove a few bases from my cloned insert using PCR - (reply: 3)
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Bisulfite sequencing of PCR products after AIMS technique - (reply: 3)
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PCR help - (reply: 1)
-
Help reamplifying the Fusion PCR - (reply: 3)
-
PCR amplification using universal 16s rDNA - it's necessary to do it (reply: 3)
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primers for bisulfite-modified DNA: general questions - (reply: 6)
-
LM-PCR amplification - (reply: 1)
-
5'-RACE PCR - (reply: 3)
-
RT-PCR NTC- substitute DNA with water? - or just end up with a smaller rxn volume? (reply: 1)
-
RT-PCR Controls (no DNA) show weird amplification - Complicated problem- urgent help needed! (reply: 4)
-
PCR protocols - for some antibiotic resistant strains (reply: 2)
-
Negative control primer for ChIP - (reply: 3)
-
How to quantitate the pcr product from gel picturess - (reply: 4)
-
inconsistent result from real time PCR - (reply: 2)
-
primers for promoter amplification - (reply: 1)
-
Cloning after amplifying with Taq polymerase? - (reply: 5)
-
RT-PCR primer designing - (reply: 6)
-
ways to get a good gene amplification - (reply: 4)
-
Scaling up PCR reactions - (reply: 4)
-
PCR with overlapping primers - (reply: 1)
-
Free program for primer designing? - Need to check promoter sequence for possible primer binding sites (reply: 3)
-
Can any one suggest a company who can design a primer pair - dnaK PCR work (reply: 1)
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cloning through PCR - (reply: 3)
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PCR doubts - (reply: 7)
-
Homemade TaqMan PCR Mastermix? - (reply: 1)
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Problem about RT-PCR for beta-actin - (reply: 2)
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My primers don't work with Chip - (reply: 1)
-
LNA Primers design - (reply: 1)
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qPCR using random primers - (reply: 4)
-
PCR optimization failure - (reply: 18)
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designing primers for cloning - designing primers for cloning (reply: 1)
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Lambda DNA nanowires, Restriction sites and thiolated primers - (reply: 1)
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no bands in PCR reaction analysis - does centrifuge time matter? (reply: 2)
-
PCR of methylated DNA? - (reply: 1)
-
PCR optimization - (reply: 5)
-
Verification of real-time amplification specificity - (reply: 1)
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1. ABI Power SYBR® Green primer efficiency? - (reply: 1)
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pcr machine - construction (reply: 1)
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Polymerase Activity Assay - (reply: 1)
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GenScript- Free PCR Reagents and DNA Purification Kits! - (reply: 1)
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About Reverse transcriptase PCR followed by PCR - primers (reply: 1)
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Amplifying a 1700bp fragment using a mismatched primer pair - (reply: 2)
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PCR inespecific band only in control - why only in the control? (reply: 2)
-
Long and Accurate PCR - (reply: 2)
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Identification by 16S rDNA - using short primer (reply: 2)
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PCR stopped working with new dNTP! - (I've tried all the usual suspects) (reply: 4)
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Degenerate Primers - (reply: 12)
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PCR buffer and PCR efficiency - buffer pH and salt (reply: 2)
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What safety and risk assessments should i be aware of in doing PCR and gel elect - (reply: 2)
-
systemic way to reduce BSP PCR bias - (reply: 1)
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restriction enzymes primers - (reply: 5)
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Plasmid DNA Sequencing with Universal Primers - (reply: 3)
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Fusion PCR - Help ragrding Fusion PCR (reply: 5)
-
need anealing temp for PCR - (reply: 8)
-
Roche produce Blunt or dA tail PCR product? - (reply: 3)
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Primer Efficiency (how to change the slope) - (reply: 5)
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Optimisation of dCAPS markers (degenerate primers) - problems with detection of heterozygotes (reply: 1)
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Inhibitory component of a PCR assay - (reply: 10)
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Ever heard not of Prime Dimers but Primer Multimers? - (reply: 1)
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PCR in 96-Well Plate - (reply: 4)
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Isolation of the upstream region of a gene by PCR: a new tecnique? - (reply: 4)
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Possible mutations in primers? - (reply: 4)
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make PCR template blunt ended - (reply: 2)
-
autoclaving tubes for PCR/RT-PCR - (reply: 5)
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AT rich PCR problems - anyone experienced with tetramethylammonium chlroide? (reply: 3)
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Quickchange site directed mutagenesis/PCR problem - Transformation isn't working :( (reply: 8)
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how would you detect a point mutation in the genome? PCR? - (reply: 3)
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How many of us request for PAGE purification of primers more than 30 mers in len - PAGE purified primers (reply: 5)
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KOD HiFi DNA Polymerase - (reply: 3)
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PCR contamination in NoRT Control - I need advice (reply: 1)
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Need to confirm PCR primers are bad - (reply: 5)
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RT PCR - NO PCR PRODUCT (reply: 3)
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PCR - (reply: 1)
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Annealing step in PCR - (reply: 1)
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Expectations for presentation of pcr data - (reply: 1)
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forgot my PCR tubes 1 h at 8°c... - (reply: 7)
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False negative PCR result - (reply: 5)
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RT PCR strange melting curve - (reply: 3)
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help with nested PCR for splice variant detection - nested PCR (reply: 3)
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PCR - (reply: 5)
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Ligation of half blunt PCR fragments - (reply: 4)
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RNA quantification for Real Time RT-PCR - (reply: 2)
-
first time doing quantitative real time PCR - (reply: 1)
-
cloning primers, TM, and specificity - (reply: 4)
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Help! Primer Dimers… - (reply: 3)
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Allele Specific PCR Primer Design - (reply: 1)
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RT-PCR without RNA isolation - (reply: 2)
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Does non-digested RNA in cDNA sample have an effect on RT-PCR quantification? - (reply: 2)
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Very low PCR primer concentrations? - (reply: 4)
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Other than Taq? - for PCR after RT (reply: 3)
-
Inconsistent PCR results - (reply: 3)
-
Question about BSP primer design? - What is the complementary strand for forward primer? (reply: 3)
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Multiplexing first round PCR in BSP - Any experience? (reply: 16)
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Locate a lab for PCR and Gel work - (reply: 2)
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PCR detectable units - PDU (reply: 2)
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Primer sets for Bisulfite-modified and unmodified DNA - (reply: 6)
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Designing forward primer incorporating Nde1 cut site - Tips on cloning with Nde1? (reply: 2)
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Real time PCR of low expressing genes - Late tumor Ct (reply: 1)
-
no results in RACE PCR - (reply: 5)
-
Help with fusion PCR to piece together fragments - (reply: 5)
-
Very resistand band in PCR - (reply: 7)
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multiplex rt pcr - (reply: 5)
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Knockdown detected by western but not RT-PCR - (reply: 3)
-
long pCR kit - (reply: 4)
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PCR Amplification from clones - (reply: 7)
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Longest Amplicon Using Real-Time PCR? - (reply: 1)
-
Primer Design for Gene Inserted Counterclockwise into Plasmid - Please help...very basic question for a mol. biologist (reply: 1)
-
real time PCR with ChIP - (reply: 4)
-
PCR cloning problem - (reply: 6)
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UV light, dangerous to purify PCR fragments? - (reply: 2)
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validation of micrarray data by realtime pcr - (reply: 1)
-
PCR DNA IMAGES ON GEL HELP WANTED - (reply: 3)
-
minimum amount of rna in RT-PCR - (reply: 1)
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Sss1 treatment of PCR amplicons - Potential dumb question (reply: 1)
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Trying to lyse cells to get PCR template - Need something simpler than a miniprep (reply: 10)
-
double digested PCR product into competent cell - (reply: 2)
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PCR Primer again - (reply: 1)
-
PCR cloning, faint band - (reply: 4)
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RAPD PCR - (reply: 1)
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False priming in MSP - (reply: 4)
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Polymerase Choice Troubles - my primer melting temp is so low (~30 C) (reply: 4)
-
PCR efficiency - (reply: 1)
-
multiplex RT-PCR - (reply: 6)
-
cDNA for real-time PCR - (reply: 3)
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cycling parameters for PCR - (reply: 4)
-
Can primers go bad and give a smear in PCR? - (reply: 12)
-
primer Tm - (reply: 10)
-
PCR product 1200bp - (reply: 3)
-
why no insert but can PCR insert out? - (reply: 5)
-
PCR cloning strategy - (reply: 4)
-
smear in degenerate PCR - (reply: 3)
-
Panomics Methylation Promoter PCR Kit - (reply: 1)
-
Single Codon Deletion - SOE PCR - (reply: 3)
-
QuickChange primers self-made - (reply: 4)
-
oligos as synthetic "miRNA" for quantification? - would an oligo / primer work in AB RT kit? (reply: 2)
-
DNase digestion step necessary for real-time RT-PCR? - (reply: 2)
-
PCR Conditions for primers with GC Clamp and without GC Clamp - (reply: 3)
-
Mystery PCR product at lower dilutions - (reply: 3)
-
PCR for checking transfection - (reply: 6)
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Non specific amplification - How to check if the primers give non specific amplification or not (reply: 4)
-
digoxygenin-labelled primer - (reply: 3)
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DNA conc for PCR - (reply: 1)
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How to import GeBank files into Primer Express 2.0 - (reply: 1)
-
Colony PCR or PCR with Growing culture in Broth - Trying to detect the cloned fragment in living cells (reply: 16)
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ChIP: I get smear after PCR? - (reply: 2)
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Why my ChIP PCR results are always unrepeatable? even from the same sample. - (reply: 7)
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Old PCR publication - help! - (reply: 2)
-
freezing of primers - (reply: 2)
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Primers with RE sites - (reply: 2)
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Smeared PCR product - ISSR marker screening (reply: 1)
-
overlap extension using PCR (3way PCR) - (reply: 1)
-
PCR - qPCR inconsistent - To explain differences between normal PCR and qPCR (reply: 6)
-
normalization for real-time PCR - (reply: 4)
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Primer dilution and calculation - (reply: 4)
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what can i do with this pcr? - amplification of cDNA , with primers tm 50 and 67 (reply: 7)
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Designing primer for Banana mild mosaic virus - (reply: 3)
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Fusion PCR for eventual TA cloning - (reply: 2)
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Ligation insert without PCR? - (reply: 6)
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improve the DNA cons. in RT-PCR - (reply: 2)
-
attaching t7 promoter sequence to template primer - (reply: 1)
-
Inverse PCR problem! plz help! - (reply: 2)
-
southern conflicts with PCR in knock-in mouse screening - why southern positives are not the mutant we want (reply: 5)
-
primer for real-time and reverse transcriptase PCR - (reply: 1)
-
PRIMER 3 PROGRAMME - (reply: 8)
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reverse transcription PCR - (reply: 1)
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Statistical analysis of quantitative real-time PCR (qRTPCR) - Statistics on qRTPCR data (reply: 2)
-
Bisulfte PCR and sequencing PCR and Primer Notes - Tips and hints on PCR for bisulfite converted DNA and bisulfite primer (reply: 33)
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primers stopped working - (reply: 3)
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RT-PCR not working - (reply: 8)
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humanized antibody - how to design primers for CDRs - humanized antibody (reply: 1)
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PCR for >4kb, i got no product. - how shud i optimize my pcr (reply: 9)
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PCR on very short sequences - (reply: 3)
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Representing RT-PCR Data - (reply: 2)
-
getting smear in PCR - (reply: 3)
-
do you ever use PAGE to check PCR? - (reply: 3)
-
Qiagen EpiTect - Kit - No PCR product after BSP, only smear! (reply: 11)
-
PCR puzzle- big or small - PCR (reply: 1)
-
Validating amplification efficiencies of the target and the housekeeping genes - (reply: 1)
-
klenowed PCR fragment into EcoRV digested bluescript - blunt end ligation proble - (reply: 5)
-
RT-PCR Question.. - (reply: 1)
-
explaining competitive PCR - (reply: 1)
-
Amplifying pathogen DNA in total DNA extractions - (reply: 2)
-
Anyone ever do a molecular beacon PCR? - (reply: 1)
-
optimization of cDNA template for real time PCR array - (reply: 2)
-
Genomic DNA PCR vs plasmid DNA PCR - (reply: 6)
-
RT-PCR kit - (reply: 3)
-
Primers going bad - what's the best storage/usage conditions? (reply: 4)
-
Weird PCR results from 2 different samples - (reply: 9)
-
5' Primer modification - Tm-effect ?? (reply: 1)
-
condition for keeping integrity of RNA for RT-PCR - (reply: 1)
-
PCR using an enzyme mix - never done this before, how do I set it up? (reply: 4)
-
Different sizes of PCR products from different competent cells - (reply: 4)
-
Designing PCR Primers - (reply: 3)
-
sequencing - which primer should I trust? (reply: 4)
-
running a gel with primers - (reply: 2)
-
Help- degenerate primer design - (reply: 4)
-
Long PCR on a cosmid vector - Help needed to run PCR (reply: 3)
-
Does set up PCR mix days prior the amplification affects the results? - (reply: 2)
-
the results of allele specific PCR is the other way around - I dont know why (reply: 1)
-
Chemically Modified Taq - Taq Polymerase (reply: 3)
-
Will this primer work? - (reply: 8)
-
Use of W primers to detect efficiency of bisulfite reactions? - (reply: 5)
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More PCR cloning problems! - (reply: 12)
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Plasmid as a PCR template - (reply: 2)
-
What are the most important parameters in PCR primer design? - Tm difference, GC clamp, GC%, primer-primer complementarity, self-complementarit (reply: 9)
-
role of MgCl2 and DTT in PCR - (reply: 3)
-
How much PCR do I need for cloning? - (reply: 5)
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Is a Kazark sequence needed in a upper primer? - (reply: 17)
-
Primers and enzymes not compatible - How can I fix this? (reply: 2)
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reampllification of pcr product - reamplification (reply: 9)
-
cytokines primers - (reply: 1)
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What's the difference between using DNA and RNA polymerase for PCR - (reply: 2)
-
How to check double digest efficiency of a linear PCR product? - Molecular Biology (reply: 8)
-
Single primer PCR - (reply: 3)
-
PCR cloning problems - (reply: 13)
-
PCR amplification of large piece from Bissulfite treated DNA - (reply: 2)
-
is there a loss of volume after pcr? - (reply: 5)
-
Inverse PCR primers design - (reply: 4)
-
Enzyme Site in reverse Primer - (reply: 3)
-
BSA concentration (and dilutions) for PCR - (reply: 2)
-
PCR product self life? - (reply: 2)
-
help as to why there are no bands when running my PCR product - (reply: 3)
-
general pcr/primer question - (reply: 1)
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Problem on PCR from cDNA - (reply: 3)
-
dephosphorylated vector and PCR insert - (reply: 7)
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2 PCR product to be inserted into 1 expression vector - (reply: 2)
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Need a FRET PCR protocol - (reply: 1)
-
size of PCR product in PAGE - (reply: 5)
-
for the PCR primer what is better the hairpin or the self annealing? - (reply: 9)
-
RT-PCR Troubles.. - (reply: 3)
-
blunt end ligation after inverse PCR - (reply: 5)
-
primers in PCR - primer removed or not (reply: 5)
-
PCR'ing a high GC gene - (reply: 1)
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Is this kind of primer OK? - (reply: 2)
-
pcr product afetr reverse transcriptase reaction - 4 bands i have not included the band which i want??? (reply: 5)
-
Real Time PCR : Bacterial gene quantification, can it be done? - (reply: 2)
-
PCR problem with CGG repeats - (reply: 4)
-
Overloading a PCR? - Is this possible? (reply: 3)
-
different primer efficiency using cDNA and plasmid/PCR product - (reply: 4)
-
RNA in cDNA - Can I use the same PCR primers for the production of cDNA? (reply: 3)
-
Primers for BS treated DNA - (reply: 5)
-
Primer Design software - (reply: 8)
-
Restriction digestion of PCR product - (reply: 3)
-
concentration of primers - (reply: 5)
-
Problems with PCR for GATEWAY - I'd get rid of 100-150bp unspecific band!!! (reply: 5)
-
Primer design - (reply: 4)
-
Pfx polymerase for site-directed mutagenesis - (reply: 2)
-
PCR product as template in another PCR - going crazy (reply: 5)
-
Nested polymerase reaction - why to do this nested PCR? (reply: 1)
-
Tac polymerase denatures at room temp why? - PCR-tac polymerase (reply: 4)
-
RT-PCR product dilution and electrophoresis - (reply: 2)
-
melting temperature in real time PCR - (reply: 1)
-
forward & reverse primers - (reply: 3)
-
Fusion protein questions - Botched deletion primer (reply: 2)
-
How to calculate DNA concentration after PCR manually - not using spectrophotometry or electrophoresis (reply: 6)
-
Real-Time PCR Question - (reply: 1)
-
Taq Polymerase storage conditions - (reply: 1)
-
PCR reaction efficiency problem - (reply: 2)
-
pGEM v pTOPO PCR products for sequencing.... Help! - (reply: 3)
-
DNase treatment of RNA prior to RT-PCR - (reply: 4)
-
role of ammonium sulphate in PCR buffer - (reply: 2)
-
Direct sequencing on BSP PCR products: problems with A and T stretches - (reply: 3)
-
Primers & probes of Applied Biosystems for real time - (reply: 2)
-
Primer walking - (reply: 2)
-
What is the optimum amount ot bases that can be deleted by PCR? - (reply: 5)
-
When I change Taq polymerase - (reply: 1)
-
Can I PCR a gene of 2KB? - (reply: 3)
-
Methyl Primer Express from ABI - (reply: 2)
-
When I chage Taq polymerase - (reply: 2)
-
PCR Optimization question - (reply: 4)
-
Target Amplicon Length for real-time PCR - (reply: 4)
-
Real-Time PCR/Melting Curve Question - (reply: 3)
-
Primer Optimiztion - can this be done in water (reply: 8)
-
DNA free RNA for PCR - (reply: 6)
-
question for the PCR to cloning construct - (reply: 9)
-
RT PCR for larger amplicon - (reply: 2)
-
Large fragments from PCR. - problems getting 3.5kb from genomic DNA (reply: 4)
-
design primer - (reply: 5)
-
Mycoplasma PCR detection in media/FBS - (reply: 6)
-
RT-PCR on 3kb fragment of viral RNA - (reply: 2)
-
increasing sensitivity and reducing primer dimmer - (reply: 11)
-
can Primers for RT-PCR be used Real-Time PCR directly? - (reply: 2)
-
Real-Time PCR Amplicon Question - (reply: 2)
-
Melting Curve/Sample analysis Question (PCR) - (reply: 3)
-
PCR reagents contaminated w/ bact - still ok for fungi? - (reply: 2)
-
PCR a 100bp fragment - (reply: 3)
-
ppt DNA directly from a digestion/ pcr - (reply: 2)
-
Can DNA polimerase amplify primers itself? - need help please!! (reply: 7)
-
primer design questions for confused - (reply: 2)
-
Silly Question about RT-PCR/Primer design - (reply: 2)
-
Anyone use phusion HF DNA polymerase? - urgent!!!! (reply: 6)
-
Can you flag-tag your sequence by PCR? - cloning shortcut (reply: 7)
-
How excess template can inhibit the PCR reaction? - (reply: 1)
-
how can I carry out this PCR profile - (reply: 4)
-
Real Time PCR and Gene expression - (reply: 1)
-
WHERE CAN I BUY A COLD BLOCK FOR PCR? - (reply: 1)
-
PCR enzyme activity-can you do 50 cycles - (reply: 2)
-
primer selection for RT prior to real time - an insiders hint!!! (reply: 1)
-
REAL TIME PCR QUESTION - (reply: 3)
-
miniprep DNA v PCR product, for sequencing - (reply: 4)
-
Which primer concentration for RT with very low RNA amounts? - (reply: 1)
-
primer concentration - (reply: 7)
-
Strange problems with B-actin amplification - (reply: 1)
-
loading control of RT-PCR - (reply: 3)
-
forgot to digest PCR insert before ligation. - what happened? (reply: 7)
-
no PCR product from genomic DNA - (reply: 7)
-
restriction site in primers urgent - (reply: 1)
-
RT-PCR primer design: Over introns and exons? - (reply: 2)
-
Preparation of template for PCR - (reply: 7)
-
Problem with colony PCR - (reply: 8)
-
primer design problems - (reply: 4)
-
Gel purification of PCR products - (reply: 2)
-
Weird PCR result - (reply: 6)
-
INVERSE PCR - (reply: 4)
-
problems with PCR from chIP material - double band PCR from chIP material (reply: 2)
-
How to get rid of longer fragment in PCR? - (reply: 1)
-
SYBR VS TAqman- What is the difference other than PRimers? - TAqman works and SYBR doesnt (reply: 1)
-
Which primers are better for colony PCR? - (reply: 4)
-
pcr yield and primer concentration - (reply: 5)
-
non-specific amplification without desired fragment - (reply: 1)
-
PCR Setup stopped working - (reply: 14)
-
ligation product- direct pcr - (reply: 2)
-
is amplification directly from my ligation reaction possible? - (reply: 1)
-
RT-PCR - not qPCR! urgent please - how to choose primers (reply: 3)
-
Primer design with restriction sites - (reply: 3)
-
Precipitate in PCR buffer w/BSA & 2-mercaptoethanol - PCR buffers (reply: 1)
-
Is a 100bp PCR product more prone to give non-specific signals in a hybridisatio - (reply: 1)
-
PCR band for water but no contamination, Digestion not working - (reply: 10)
-
help PCR of GC rich templates - (reply: 3)
-
Control PCR in Ligation - Genomic DNA + linker ligation (reply: 1)
-
I am so disappointed that I failed in PCR again and again - (reply: 4)
-
Why there is use of only a single primer in case RAPD amplification - (reply: 1)
-
differences between oligo and random primers - (reply: 2)
-
overlap PCR - (reply: 5)
-
My PCR product is 100bp (approx). What result is more reliable-gel or hybridisat - (reply: 5)
-
cloning experimental design to ligate three PCR products into one plasmid - (reply: 4)
-
Why is it difficult to PCR taget gene in rice successfully ? - (reply: 1)
-
dNTP calculation - (reply: 3)
-
PCR contamination - (reply: 2)
-
RT-PCR primers - (reply: 3)
-
Effect of Temperature on PCR - (reply: 3)
-
How does isopropanol inhibit PCR? - (reply: 4)
-
Difficulties getting a 4 kb PCR product - (reply: 5)
-
Yet another PCR problem/question - (reply: 11)
-
PCR product multiple bands - (reply: 3)
-
PCR BLOck contamination? - better anti-contaminant PCR - tube? (reply: 15)
-
Any primer design programs...? - (reply: 8)
-
Problem SNP that genotypes differently using different primers? - (reply: 2)
-
Which result is correct-Western or RT-PCR - (reply: 5)
-
Transforming after digesting PCR product - (reply: 6)
-
Cutting out of a T vector - Cutting sites in primers vs sites in vector (reply: 3)
-
Standard PCR banding? - multiple bands instead of one (reply: 4)
-
PCR problems, huge artifacts, no product - involves 16S primers (reply: 8)
-
primer : shifting peak - (reply: 4)
-
rt-pcr data and western blot data not compatible - what could be the explanation (reply: 5)
-
about RAPD PCR of plant genomes? - (reply: 4)
-
Touch down PCR - (reply: 8)
-
PCR ...introduction - (reply: 16)
-
RealTime PCR of microRNAs - (reply: 9)
-
RT-PCR of apoptosis related genes - (reply: 2)
-
Primer design for BSP - (reply: 12)
-
gDNA salvage for PCR from mounted tissue sections - Is it possible? (reply: 1)
-
Designing primers and hybridization probes - (reply: 1)
-
HMW band in well after bisulfite PCR - (reply: 1)
-
Junk/dimers on left of single product peak - (reply: 3)
-
Random Primers vs Oligo(dT) primers? - (reply: 3)
-
gel purification of PCR product - (reply: 1)
-
Is all lab bacterial strains have t7 RNA polymerase gene... - (reply: 4)
-
RT PCR Primer - Software (reply: 2)
-
ChIP primer for promoter region of GAPDH - for taqman analysis (reply: 2)
-
Possible to clone when you have only 20ng PCR product? - (reply: 10)
-
5' phosphorylated primers - (reply: 1)
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Increased signal in IP after peptide addition? - Immunoprecipitation signal amplification (reply: 2)
-
Methylation specific primer designing - (reply: 1)
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How to PCR a 100bp fragment - (reply: 4)
-
primer design with intentional mismatch - (reply: 3)
-
Problems with PCR following bisulfite treatment - (reply: 11)
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Amplifying a 6.5 kb cDNA - (reply: 3)
-
pBluescript cloning of PCR products - (reply: 1)
-
Ligating blunt adapter to PCR product - (reply: 7)
-
Primer Extension Assay versus RACE-PCR - Protocol (reply: 1)
-
RT-PCR problems on mouse ear RNA - (reply: 1)
-
vector PCR problem - stuck in experiments... (reply: 2)
-
promoter methylation PCR kit from Panomics - (reply: 2)
-
please tell me more about primers with restriction site! - (reply: 4)
-
PCR 3kb fragment - (reply: 3)
-
Problem in Patch PCR for Site-Directed Mutagenesis - (reply: 5)
-
RT-PCR primer design - (reply: 1)
-
transgenic mouse - identification by PCR (reply: 2)
-
Primers work for regulary PCR but not real-time PCR - why? (reply: 8)
-
pcr detection of pathogens - (reply: 3)
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how to check primers - (reply: 4)
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Recombinant PCR - (reply: 5)
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PCR after in vitro transcription and translation - (reply: 2)
-
standard curve and differentiation asays - Real Time PCR (reply: 2)
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[PCR] Which substances cause inhinbition of Taq? - (reply: 5)
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[PCR] Different amplification-efficiency of varying DNA - (reply: 1)
-
troubles in PCR amplifying long target - (reply: 4)
-
allele-specific amplification - (reply: 1)
-
PCR clone a gene with known 3' end only - (reply: 4)
-
Double bands in PCR - WHY? - (reply: 5)
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PCR Cloning - (reply: 3)
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Long range PCR - What enzymes do you use? - (reply: 6)
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Bis. PCR not working. MSP is fine - (reply: 1)
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sear in PCR no bands - (reply: 3)
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How to design primer for unknown DNA sequence? - (reply: 9)
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Few colonies with cloning of PCR product after digestion - (reply: 7)
-
TM for primers with restriction secuence tail. - Suggestion (reply: 3)
-
can primers age? - (reply: 1)
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How to determine PCR Annealing temperature for primers with different Tm - (reply: 7)
-
No PCR Product after Bisulfite Modification - (reply: 5)
-
poor random priming for Northern Blot probes - (reply: 1)
-
PCR with 75 mer forward primer - (reply: 4)
-
strange RT-PCR expression - (reply: 1)
-
half life of primers - (reply: 2)
-
PCR band disappears in agarose gel! - Agarose gel electrophoresis (reply: 4)
-
competition of multiple PCR products - (reply: 1)
-
MOLECULAR TEST WITH !JUST PCR AND GEL! FOR A STARTER - PLEASE GIVE ME SUGGESTIONS (reply: 3)
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PCR from Genomic DNA - (reply: 3)
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Problem with the PCR Product and Extraction - (reply: 2)
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about the primers in MSP - (reply: 5)
-
SYBR green problem.. - real time PCR SYBR (reply: 2)
-
ARMS PCR - (reply: 3)
-
Why do a nested PCR? (HIV virus) - (reply: 4)
-
cloning problem with pcr and pegfp vector - (reply: 9)
-
Should I clone my PCR product even though it is invisible on gel? - (reply: 5)
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What annealing temperature is better for my primers? - (reply: 7)
-
primer dimer in pcr product - cloning for a gene. analyzing pcr product shows primer dimer (reply: 8)
-
primer concentration (calculation problem) - (reply: 5)
-
PCR, labelled vs unlabelled primers - (reply: 4)
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Problem with cloning p53-suggestions for RT-PCR - (reply: 1)
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How to add restriction enzyme sites to the primer - (reply: 6)
-
PCR: same premix, same everything, different results... - (reply: 21)
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Using pentadecamer primers for reverse transcription - Better than hexamers, oligo d(T)? (reply: 7)
-
How to confirm a 80bp PCr fragment? - (reply: 5)
-
pcr grape vine - (reply: 1)
-
RT-PCR control for Vitis vinifera - (reply: 2)
-
PCR shows insert, but digestion of plasmid failed to cut out insert - (reply: 2)
-
Problem PCR amplifying gene promoter regions - (reply: 4)
-
Problem amplifying 8kb bacterial genomic DNA - (reply: 2)
-
pGEM-T Restriction Enzymes won't cut out PCR clone - (reply: 3)
-
syber green with real time PCR - (reply: 17)
-
primer:cross-dimer - How to remove the cross dimer? - (reply: 3)
-
Got different size PCR products from chIP - (reply: 7)
-
PCR trouble.....help! - (reply: 16)
-
Re-amplify PCR product by realtime PCR? - (reply: 13)
-
My PCR's are killing me! - nothing is working!! (reply: 9)
-
pcr product transfection help - (reply: 3)
-
PCR almost like false positive problem! - How can I get rid of 5bp band near mine !!!!!!! (reply: 2)
-
Bands appear poor/not at all and do not appear consistantly & primer bands a - (reply: 2)
-
dNTP dilution for PCR - (reply: 4)
-
housekeeping gene in real-time PCR - (reply: 2)
-
can I detect colony for the insert with the cloning primers? - or clamp sequence will interfere? (reply: 4)
-
Constant amplification in PCR negative control - (reply: 2)
-
alternative to dmso in pcr - (reply: 3)
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Hemin amplifying ECL signal?!? - (reply: 5)
-
The weirdest primer ever - (reply: 7)
-
oligo(dT) plus random primers in RT - (reply: 4)
-
Trouble with real-time PCR standard curve - (reply: 4)
-
PCR inhibitors - PCR inhibitors (reply: 1)
-
no RT controls - can I run on separate plate and for just one primer set? (reply: 1)
-
primer calculation - concentration (reply: 2)
-
What happens to PRIMERS at 72 C ? - (reply: 5)
-
Colony PCR was carried out following lysis of cells with Igepal CA - 630 .. - But how? (reply: 2)
-
PCR cleanup - Quick question (reply: 1)
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0,2uM is 100ng of a 18-mer primer - (reply: 8)
-
No PCR product detected in agraose gel - (reply: 7)
-
PCR problem - 1.8 kb fragment amplification (reply: 3)
-
2 melting peaks in real-time PCR - (reply: 1)
-
PCR amp. - sequencing problem - (reply: 3)
-
visualizing unknown DNA with linkers and PCR - (reply: 2)
-
Difference between MgCl2 and MgSO4 in PCR? - (reply: 4)
-
DNA fingerprinting - Is it necessary to use DNA polymerase with proof-read function in PCR? (reply: 2)
-
Melting Curve giving flutating Ct values - Advice on primer design? (reply: 9)
-
checking colonies by vector primers.... - (reply: 7)
-
Pfu polymerase from promega - (reply: 4)
-
Does 2-mercaptoethanol inhibit PCR reactions? - anyone know? (reply: 7)
-
PCR: annealing temperature - (reply: 3)
-
Nested PCR troubleshooting - no secondary product - (reply: 5)
-
Direct BSP using tag-modified primers - (reply: 2)
-
adding restriction sites to degenerate primers - (reply: 9)
-
PCR: multiplex ok, single reactions not - microsatellite analysis (reply: 2)
-
Two to use PCR to get domain deletion within a protein? - (reply: 2)
-
Added DNTP solution to DNA by mistake - (reply: 3)
-
Standard vs High fidelity polymerase, please help - No results with high fidelity (reply: 5)
-
Mutagenesis using 4 sets of primer - (reply: 6)
-
PCR on a GC rich region - PCR on a GC rich region (reply: 4)
-
Relative Quantification in real-time RT-PCR - (reply: 5)
-
PCR amplification of Community DNA - (reply: 6)
-
library titering and amplification - (reply: 1)
-
Unwanted band seen along with my pcr product. - regarding PCR product with unwanted band formation during electrophoresis (reply: 3)
-
Wierd amplification pattern. - (reply: 8)
-
cloning primer and tag questions - first try (reply: 2)
-
nested PCR: purification? - (reply: 1)
-
PCR problems with 1,7kb fragment - (reply: 8)
-
Question about bisulfite PCR - (reply: 2)
-
reuse PCR gel - (reply: 2)
-
PCR analysis of clones - Can a gene specific primer pair amplify a fragment in the wrong direction? (reply: 1)
-
Amplification of gene (CHH,MIH,GIH) from prawns. - Amplification of gene using primers designed on the basis of cDNA sequences (reply: 1)
-
pro-PCR with only one primer... - to check directionality. (reply: 4)
-
Two design programs give very different primer Tm values - RT-PCR (reply: 5)
-
Wrong sized PCR band following digest & ligation into vector - :( please help... (reply: 1)
-
Problem of Smear - Smearing of PCR product (reply: 7)
-
Inconsistent results from replicates in Taqman real-time PCR - (reply: 26)
-
cDNA synthesis primer - (reply: 3)
-
Amplification of phage library - (reply: 3)
-
gsamsa - Gene array vs PCR (reply: 4)
-
Primer with tag: Which is the real concentration? - (reply: 3)
-
Any one can tell me what happens to my RT-PCR? - Urgent !RT-PCR really kills me! (reply: 5)
-
PCR Trouble - (reply: 5)
-
PCR of herbarium specimes - PCR of Caesalpinia herbarium specimes (reply: 1)
-
Problems (unspecific products) with PCR to determine the size of cDNA inserts - (reply: 7)
-
pcr product transfection - (reply: 8)
-
antigen primers - (reply: 1)
-
restriction digestion of PCR product? - (reply: 10)
-
How to design PCR primers in ChIP assay - (reply: 2)
-
Is the insert not complete? - Sequencing Cloned PCR product (reply: 5)
-
Annealing vs melting Ts for real time PCR primers - (reply: 1)
-
Taq polymerase vs HotstartTaq polymerase - (reply: 4)
-
what hybridization temp in pcr - (reply: 5)
-
relative quantification, primer pair problem - (reply: 1)
-
Pfx PCR problem - (reply: 6)
-
Question about PCR reaction condition - (reply: 3)
-
RNA Amplification - (reply: 2)
-
PCR Internal Controls - (reply: 2)
-
Calculating Tm for bisulfite primers? - (reply: 3)
-
smear in PCR - No consistancy in amplification (reply: 3)
-
real-time PCR for quantitation of MSP - (reply: 3)
-
Designing species specific primers for E.coli - please help? (reply: 3)
-
DMSO Contamination in PCR - (reply: 3)
-
Chloramphenicol amplification - (reply: 5)
-
Fusion/overlap PCR troubleshooting - (reply: 3)
-
Screening a Gene Library - I want to use colony PCR, but How (reply: 4)
-
how could one avoid amplification of a very high non-specific band from PCR - (reply: 3)
-
Using primers meant for DIG probe as PCR diagnostic - (reply: 1)
-
Using primers meant for DIG probe as PCR diagnostic - (reply: 3)
-
Need for Nested PCR - Primers Designed with MethPrimer - (reply: 6)
-
Real time PCR for gene family - (reply: 3)
-
single restriction enzyme digestion? - is it possible to insert PCR product? (reply: 17)
-
Do I have to make pcr master mix fresh every time - (reply: 1)
-
2nd round of amplification issues - (reply: 1)
-
Topo Zero Blunt Vector by Promega Amplification of insert with M13 - Amplification of insert with M13 primers (reply: 1)
-
Smearing of the PCR Products - (reply: 10)
-
Primer for 5' RACE - (reply: 2)
-
Stick T7 on custom primer for sequencing? - (reply: 2)
-
RNA polymerase? - (reply: 5)
-
SMEAR IN POSITIVE CONTROL IN LONG PCR - (reply: 3)
-
To dephosphorylate the vector or not? - For cloning PCR product (reply: 6)
-
Cloning PCR product - Any ideas? (reply: 3)
-
ABI have released MethylPrimer Express! - A new primer design program for DNA methylation....For Free!!! (reply: 45)
-
MSP primer design help - (reply: 5)
-
PCR using long primers and two overlapping templates - PCR using long primers and two overlapping templates (reply: 2)
-
Primers for nested-PCR - (reply: 1)
-
PCR primers with high Tm - (reply: 6)
-
no product after PCR - (reply: 5)
-
how to choose best annealing temp. for primers? - (reply: 6)
-
Primer Dimer problem- Different perspective - COuld there be a treatment effect (reply: 4)
-
PCR using a long (100nucleotides) and a short (20 nucleotides) primer. Problem: - (reply: 7)
-
making primers for similar protein sequences - making primers for similar protein sequences (reply: 4)
-
PCR quickchange with high Tm oligos - help needed (reply: 2)
-
BSP and MSP Primers - (reply: 2)
-
PCR mixing - First tubes generally work, last ones generally don't. (reply: 3)
-
PCR question, need help please! - (reply: 5)
-
Storage of PCR product? - (reply: 1)
-
Bisulfite sequencing primer - (reply: 4)
-
MSP Primer Sets (Herman Papers) - (reply: 1)
-
specific loci not present depending on DNA extraction method? - DNA extraction and succesful PCR (reply: 1)
-
Can pfu Polymerase make a blunt end? - (reply: 3)
-
Methods for ligating fragments to form dimers.. - (reply: 1)
-
real time PCR machine choice - (reply: 1)
-
Must all BSP be nested PCR? - (reply: 4)
-
random primers for qPCR - (reply: 3)
-
QPCR, where to start? - optimizing primer and template (reply: 5)
-
difficulty in Primer walking - (reply: 2)
-
about nested PCR - (reply: 2)
-
PCR primers Tm higher than extension T - (reply: 8)
-
Primer for sequencing - need help!!!!!!!!!! (reply: 6)
-
Primer Design - (reply: 2)
-
Primer design invert pcr - (reply: 5)
-
fetal mistake in my hot start PCR - (reply: 3)
-
Standard PCR - (reply: 3)
-
cloning two fragments with deletion in between - PCR primer design (reply: 3)
-
Left my PCR supplies out overnight. Are they all ruined? - (reply: 4)
-
PCR not works time to time - (reply: 2)
-
faster way to identify RNA virus other than RT-PCR? - (reply: 2)
-
RT-PCR a GC Rich (68%) gene (2200bp) - (reply: 6)
-
Vector construction - Can I use long PCR primers (60bp) and get good PCR poduct??? (reply: 4)
-
Two bands on RT-PCR product - (reply: 8)
-
designing primers for Real Time - (reply: 1)
-
RT-qPCR of bacteria mRNA from sludge - RT-PCR, Real-time PCR, mRNA, sludge (reply: 3)
-
Stem loop RT-PCR for miRNA quantification - how can I design the stem loop primer? (reply: 2)
-
Duplicate PCR: specific bands but different sizes. - (reply: 2)
-
Real time PCR late amplification - (reply: 6)
-
4 deg Celsius after PCR - (reply: 1)
-
PCR anealing temperature question - (reply: 12)
-
PCR buffers for Taq and Pfu polymerase - (reply: 6)
-
Taq and Pfu polymerase give different amplification - (reply: 8)
-
Cloning a PCR product after digestion - (reply: 7)
-
Methods for primer reconstitution - (reply: 23)
-
Smearing in "Overlap Extension PCR" - (reply: 1)
-
Help on PCR purification - (reply: 2)
-
ASAP: ONE STEP Real time RT PCR kit for TWO step RT-PCR method? - (reply: 1)
-
BSP Primer placement over KNOWN unmethylated CpG's - Can this be done? (reply: 3)
-
differences between PCR and Quick Change PCR - what are thedifferences between PCR and Quick Change PCR? It's urgent (reply: 2)
-
Troubleshooting PCR contamination - (reply: 13)
-
ribosomal binding for pcr product cloning - urgent!!! (reply: 2)
-
no result with pcr. is it the primer?/ - no amplification in pcr even after starting from the beginning (reply: 6)
-
Digesting PCR products - (reply: 2)
-
PCR result: Nothing! - Urgent! (reply: 2)
-
RT-PCR mouse RNA released from complement-lysed cells - Goal: to whether RNA is of nuclear or mitochondrial origin. Planning to PCR ampl (reply: 2)
-
PCR large fragments - (reply: 2)
-
dimers of dna (not primers) following digest or pcr? - (reply: 11)
-
can we add the terminaton codon in the 3' primer? - (reply: 1)
-
Question about Realtime PCR primer concentration.... - (reply: 5)
-
PCR probes for Southern blot - (reply: 1)
-
Smear in PCR - (reply: 5)
-
Cloning with real time PCR fragments - using SyberGreen from Applied Biosystem (reply: 3)
-
PCR amplification - (reply: 2)
-
designing primer for methylation - (reply: 21)
-
plasmid amplification - exons and primers (reply: 1)
-
Primer dimers?Contaminations? - Unexpected bands! (reply: 5)
-
reverse primer design with restriction site - (reply: 6)
-
Reverse Transcription with oligo dT or hexamer primers? - What do you prefer and why? (reply: 3)
-
PCR dry mixture - (reply: 3)
-
Use PCR products to determine efficiency of amplification? - (reply: 7)
-
MSP PCR - (reply: 2)
-
Band in negative PCR control - (reply: 25)
-
Different RNA sources, Different PCR optimal condition? - (reply: 5)
-
question in 5' RACE and primer extesion - (reply: 8)
-
PCR contamination - does autoclaving help? - (reply: 7)
-
Primer concentration ? - (reply: 2)
-
PCR and DMSO - (reply: 2)
-
PCR my cDNA & got nothing - (reply: 2)
-
Dimer of PCR products? - (reply: 2)
-
PCR product dimer (not primer dimer!) - PCR (reply: 2)
-
Taq/PFU polymerase A overhang - bad for blunt ending? (reply: 3)
-
Degradation of PCR product during purfication - Purification of PCR product for cloning (reply: 2)
-
BAC clone amplification - (reply: 1)
-
Nonspecific PCR amplification? - (reply: 2)
-
QIAquick PCR for preparing for restriction digestion - very low concentrations (reply: 4)
-
Plasmid PCR - (reply: 5)
-
pcr products wont give me colonies - (reply: 3)
-
Nested allele-specific PCR - (reply: 1)
-
No PCR product for genotyping - (reply: 2)
-
problems in subcloning PCR products for TA cloning - (reply: 4)
-
Q-PCR questions: Primer design and melting curve - (reply: 13)
-
no product for promoter genomic PCR - (reply: 3)
-
MgCl vs MgSO4 for PCR - (reply: 2)
-
from which strand to derive BSP primers? - (reply: 5)
-
Validating microarray results - Real-time RT-PCR (reply: 1)
-
SMear instead of PCR product - (reply: 3)
-
PCR - free primer designation program (reply: 2)
-
Best product size for real-time RT-PCR - (reply: 4)
-
No success with PCR cloning of a gene into expression vector - (reply: 5)
-
what is the principle of gradient PCR? - How does it work (reply: 2)
-
Primer Annealing for PCR - (reply: 4)
-
Why is my smaller band too faint? Genomic PCR not working! - Just trying to genotype some mice... (reply: 2)
-
cDNA library screening with 5' specific primer - (reply: 1)
-
Removal of PCR inhibitor - (reply: 3)
-
Site-Directed Mutagenesis- Doubt - Overlapping primers (reply: 3)
-
Both the PCR primers in a vial. - Did anybody mix the diluted primers in single tube for use? (reply: 7)
-
PCR mix and DEPC water - (reply: 2)
-
Concentrating PCR product - (reply: 9)
-
PCR inhibitors - What are common pcr inhibitors (reply: 9)
-
How to design primer for sequencing unknown DNA - (reply: 5)
-
PCR contaminant - (reply: 4)
-
PCR mix and DEPC water - (reply: 2)
-
PCR - forward, reverse primers - is the reverse primer the "reverse complement" of the sense strand (reply: 2)
-
need helps on probe design--human ip10 primers and probe. - (reply: 2)
-
another PCR question - (reply: 12)
-
PCR - (reply: 8)
-
PCR doesn't work! - Falling in an empty gel "space" (reply: 2)
-
Success with Direct Sequening of Bisulfite Pcr Products - (reply: 47)
-
PCR contamination false positives - (reply: 6)
-
how to determin the Annealing Temp of ristriction sites modified primer? - help me ! (reply: 26)
-
Sequencing Primers - (reply: 4)
-
two bands of one gene in PCR - (reply: 8)
-
5' RACE - gene specific primer - (reply: 1)
-
RT PCR on ALM patients - help for designing primers for detect PML RAR (reply: 2)
-
Viral RT PCR - (reply: 2)
-
About PCR primers' concentration - (reply: 2)
-
Reliability of PCR? - (reply: 4)
-
Multiple unknown amplification products - (reply: 2)
-
PCR in 25 uL is it sufficient? - (reply: 6)
-
Qiagen Gel Extraction of PCR product - (reply: 7)
-
Primer design with incomplete sequence - (reply: 2)
-
Problem with lids to 8-strip .2 ml PCR tubes - (reply: 3)
-
Annealing temperatures for long primers? - PCR reaction (reply: 6)
-
Measuring the amount of PCR product - (reply: 9)
-
PCR primers from amino acids? - (reply: 1)
-
difficult PCR - (reply: 1)
-
Some Questions about PCR - ... based von Wikipedia article (reply: 1)
-
Low PCR product for antibody gene - (reply: 4)
-
chronic PCR contamination - (reply: 11)
-
Colony PCR positive, miniprep negative? - (reply: 9)
-
TA cloning: if PCR product is not freshly prepared - (reply: 2)
-
RT-PCR machine/setup problems - (reply: 2)
-
Minimum amount of RNA for real-time PCR - (reply: 4)
-
Primer dimers - (reply: 1)
-
RT-PCR, DNA contaminant removal by digestion with restriction enzyme - (reply: 3)
-
troubles with human genomic DNA amplification - (reply: 1)
-
PCR vs biochemical tests - which one is more reliable? (reply: 6)
-
RT-PCR question - genomic DNA amplified with RNA (reply: 9)
-
DNA amplification for ChIP-on-chip - (reply: 1)
-
Preserve PCR mix - (reply: 3)
-
genomic dna in real-time pcr - (reply: 3)
-
problem concerning PCR Test after disruption and yeastgenome DB - (reply: 6)
-
More about PCR dimers! - (reply: 1)
-
primers design for mutagenesis of two nearby sites - mutations (reply: 2)
-
HELP! I have a PCR amplifing problem - PCR amplifing problem (reply: 4)
-
Asymmetric PCR - (reply: 2)
-
Purify integrating PCR product before transforming yeast? - (reply: 1)
-
PCR of long fragment(approx 8 kb) - (reply: 3)
-
What does the term "smear" mean in PCR ? - (reply: 3)
-
PCR..HELP - band in no template control (reply: 1)
-
RT-PCR Control Reactions - Need suggestions! - (reply: 1)
-
Troubleshooting PCR smear - Urgent,Need help! (reply: 4)
-
Reamplifying my PCR product - (reply: 7)
-
[urgent help] Band missing in PCR - (reply: 5)
-
DNase I Amplification grade and DNase I for RNA treatment - (reply: 1)
-
Multiplex PCR - (reply: 4)
-
design spesific primer of avr, hrp, toxin and falgella gene - (reply: 3)
-
Smearing in nested pcr product - (reply: 2)
-
no pcr product with pfu/pwo but with taq - (reply: 3)
-
Intensive primer dimers - (reply: 2)
-
pcr contamination - (reply: 3)
-
PCR using different primers to generate same DNA sequence - explanation please :) (reply: 2)
-
PCR problem: long product (4 kb) from a cDNA library - (reply: 2)
-
PCR no longer works - no pcr product? (reply: 3)
-
quantifying cDNA for Real Time PCR - (reply: 3)
-
What should I do for more samples need to be tested by real-time PCR? - (reply: 1)
-
no band after long-distance PCR - (reply: 3)
-
Laddering effect in PCR blank control - (reply: 4)
-
PCR is positive with one set of primers, negative with another. - (reply: 4)
-
Do you synthsize your own oligo(dT) primer? - (reply: 2)
-
Can't get MSP PCR products at all after treatment! - Help with MSP using Chemicon Fast DNA Mod Kit (reply: 1)
-
PCR on Genomic DNA - (reply: 2)
-
Trouble with primers of BSP - (reply: 3)
-
Could higher ammount of taq be inhibitory for overall PCR reaction? - (reply: 2)
-
Touchdown PCR for MSP? - (reply: 4)
-
genotyping mice-no pcr product - (reply: 3)
-
PCR smears are getting me crazy! - (reply: 1)
-
Nested PCR - no amplicon - (reply: 1)
-
PCR from pit soil type DNA sample - (reply: 3)
-
PCR - (reply: 3)
-
degenerate primer design - (reply: 4)
-
Volume of Real time PCR mastermix and reaction - (reply: 4)
-
Decreasing Amplification Curve for Standards - (reply: 2)
-
Weird duplex PCR results - (reply: 5)
-
Home-made Sybr green mix for real-time PCR - (reply: 1)
-
PCR - (reply: 4)
-
PCR buffers - can I use MgCl2 alone (reply: 4)
-
potassium acetate in primer solution - I made a mess but need to recover (reply: 6)
-
RNA storing/RT PCR using oligo dT - (reply: 5)
-
cloning/amplifying attenuate RNA transcripts - (reply: 6)
-
PCR with attB not working - (reply: 1)
-
Nested PCR problems - (reply: 1)
-
Very, VERY weird PCR results! - (reply: 4)
-
confirmation of my pcr product - (reply: 2)
-
What is the advantage of nest PCR in methylation analysis - (reply: 1)
-
16S rRNA primers for E. coli - (reply: 2)
-
Insert size longer than expected on PCR - (reply: 3)
-
About PCR smear - Anyone can help me? (reply: 4)
-
preferential amplification among transcripts - (reply: 1)
-
primer design - how to design primers (reply: 2)
-
Should I dilute cDNA for real-time PCR? - (reply: 3)
-
Real-time PCR problems - RT_PCR (reply: 7)
-
PCR cloning problem - No colonies - (reply: 10)
-
HIV RT PCR KIT - (reply: 1)
-
strange contamination in real-time PCR in negative control? - (reply: 1)
-
Real time PCR - no product - (reply: 1)
-
Impact of temperature and time increment during PCR - (reply: 3)
-
Multiplex Primers - Primer primer interaction (reply: 1)
-
dNTP degradation - (reply: 4)
-
Housekeeping gene for RT-PCR on plant - RT PCR (reply: 1)
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inconsistent PCR results - (reply: 2)
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PCR smear in samples and negative control - (reply: 5)
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pcr sequencing - (reply: 2)
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How should I check my colonies? - PCR check is not working...:( (reply: 5)
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RT-PCR of an intron - possible plateau effect? (reply: 2)
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question about mutagenic PCR. - (reply: 2)
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Why primers for bisulfite converted DNA amplify unconverted DNA? - (reply: 3)
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phenol/chloroform of purified PCR product after RE digestion - what are we trying to purify? (reply: 4)
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SYBR Green PCR Master Mix storage - (reply: 3)
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PCR and topo problem - (reply: 3)
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RT-PCR primer design at 3'-UTR or ORF? - (reply: 2)
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Reverse transcription of poly-A tailed miRNAs using anchored Oligo dT primers? - (reply: 6)
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is PCR credible enough for validating my clones? - (reply: 5)
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How to calculate absolute fold change in expression by realtime PCR - Realtime PCR (reply: 2)
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unknown PCR bands - (reply: 4)
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Amplification of 3KB protein from Hela mRNA PCR PROBLEM - PCR Amplification of 3KB protein (reply: 6)
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Problem amplifying DNA from tissue - (reply: 4)
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qPCR for HKG and traditional PCR for GOI - (reply: 1)
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PCR or digestions for clone screen? - (reply: 5)
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Smeary bands in real-time RT-PCR - (reply: 7)
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high GC content in PCR? - (reply: 2)
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RT PCR - (reply: 1)
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Amplification of specific genes from cDNA - (reply: 3)
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How to purify PCR product? - (reply: 3)
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Touch down real-time PCR? - (reply: 1)
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PCR internal control - how does it work? (reply: 1)
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Primer design for environmental samples - Align sequences first? (reply: 3)
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False positive for PCR screening of insert - (reply: 1)
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not able to ligate PCR product into a vector... - what do you suggest? (reply: 2)
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why using Vent-exo polymerase? - (reply: 2)
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southern hybridizaion with 5' end labelled primer - (reply: 1)
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Programs for designing Primers - (reply: 6)
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DNA template for PCR reaction - (reply: 6)
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Disadvantages of using oligo-dT primers - (reply: 1)
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PCR chemistry - (reply: 4)
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Selective amplification problem in AFLP - (reply: 1)
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shorter PCR products after bisulfite treatment and cloning - (reply: 5)
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my insert is there by PCR check but no band after digestion... - vector not digested because of contamination? (reply: 3)
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Stool PCR and RFLPs - Campylobacter PCR from Stool (reply: 6)
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Do I need internal controls in MS-PCR? - Methylation specific PCR Internal controls (reply: 3)
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Blunt PCR cloning not working - (reply: 2)
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PCR Trouble shooting - PCR Trouble shooting (reply: 2)
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Genomic DNA Contamination of Real Time PCR - (reply: 4)
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ES cell genomic DNA as PCR template for screening - (reply: 5)
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How to eliminate primer dimer in MSP - (reply: 20)
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Problem with PCR amplification - (reply: 2)
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Band diffusion of my PCR product in electrophoresis - (reply: 3)
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Simple PCR - (reply: 1)
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do primers and dNTPs alter digestion efficiency? - (reply: 4)
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targetted pcr - targetted pcr (reply: 3)
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PCR from human genomic DNA - (reply: 4)
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Sequencing primer dilution - (reply: 2)
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magic? - got more product after PCR purification... (reply: 3)
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PCR for cloning - PCR (reply: 2)
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Optimization of PCR annealing temperature - (reply: 7)
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PCR with degenerate primer - (reply: 6)
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Strange PCR bands behaviour - (reply: 2)
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1.3kb PCR only shows primer dimer - (reply: 2)
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Problem with PCR on DNA from paraffin section - (reply: 2)
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Titration of Mg2+ in RT-PCR - (reply: 3)
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RFLP PCR amplification - No amplification in PCR (reply: 2)
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RT-PCR primers for E. coli LacZ gene - (reply: 3)
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water instead of TE buffer to dissolved primers - (reply: 6)
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SOS: real time PCR standard curve - (reply: 1)
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Addition of pcr reagents to master mix - What order is best? (reply: 1)
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Serratia PCR - (reply: 6)
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primer reconstitution - (reply: 2)
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QuickChange mutagenesis: how to do it without kit? - What dNTP concentration should I use? (reply: 1)
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Question about PCR primer with degenerate base at 3' end - (reply: 2)
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Long distance (16 kb) PCR problem - (reply: 12)
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methylation Primers - Methyalted PCR (reply: 1)
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Primer for 4 genes sharing short consensus sequence - (reply: 2)
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what is the best pair of sequencing primer for puc 18 - (reply: 1)
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Looking for online primer design for SNaPshot - (reply: 1)
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pCI sequencing primer - (reply: 1)
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ask for an explanation to pcr ladder at high cycle number - help (reply: 2)
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about designing PCR primers - help (reply: 3)
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PCR primers: hairpin and dimers? - what can I do to avoid this? (reply: 4)
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1st time real-time PCR questions - (reply: 1)
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BSP - favors amplification of unmethylated template? - (reply: 2)
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real-time pcr optimization problem - (reply: 4)
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PCR on PCR of cDNA smear - (reply: 1)
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RT-PCR amplification of an intron - has anyone tried this? (reply: 4)
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Reconstitute primers - (reply: 4)
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Which polymerase for bisulfite sequencing PCR - (reply: 3)
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PCR product - (reply: 5)
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Problems in reproducing the PCR results! - conventional PCR (reply: 3)
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Delta-delta Ct method and PCR efficiencies - (reply: 9)
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Multiplex PCR Problem - SOS (reply: 3)
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multiplex PCR for three sets of primers - (reply: 1)
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attach adaptors or PCR the restriction enzyme sites? - which one would you suggest and why (reply: 2)
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repeat PCR amplification problem - (reply: 2)
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PCR product purification - (reply: 3)
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to purify these PCR products or not? - preparation for restriction digest (reply: 5)
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inner primer for BSP PCR? - (reply: 6)
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How many mismatches in point mutation primers? - (reply: 3)
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Direct DNA sequencing - sequencing without PCR product (reply: 6)
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Software available for Multiplex PCR primer designing - (reply: 3)
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Picking stable clones by RT-PCR.. - (reply: 2)
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PCR of ligation products - (reply: 8)
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single primer PCR - use a single primer to amplify regions between inverted repeats (reply: 1)
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multiplex pcr trouble - some bands won't amplify (reply: 16)
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PRIMER design - primer dimers (reply: 1)
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Subcloing PCR fragments - (reply: 1)
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Why I keep getting no colonies from transformation of PCR products - help! (reply: 5)
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3' - 5' activity of Taq DNA Polymerase - (reply: 2)
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ACE PCR - problems with PCR for angiotensin-converting enzyme (reply: 2)
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Amplify 4.5 kb pcr product without using special polymerase - (reply: 10)
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PCR master mix - (reply: 6)
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SOS! asymmetric PCR, no PCR product - (reply: 2)
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degenerate PCR vs low stringency PCR - (reply: 1)
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RT-PCR- help - Polyacrylmide Gel electrophrosis for PCR products (reply: 3)
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No DNA on gel, but get PCR product - (reply: 2)
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Mouse MSP primers - (reply: 11)
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PCR primer: 2 restriction sites? - (reply: 4)
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Primer Dimer problems in real-time PCR - (reply: 14)
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No PCR Product - Fungal Genomic PCR (reply: 9)
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primer orientation - (reply: 1)
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need help,why colony pcr of my blue has product what i need - (reply: 2)
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Degenerate primers for nested PCR? - (reply: 1)
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so lost! stupid quenstion about primers.... - designing the primers (reply: 2)
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Looking for real time PCR workshops - real time PCR workshops (reply: 2)
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Amplification of the uncharacterized regions by Inverse PCR - what's the application since the target gene is inverted after it? (reply: 2)
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Reliable ChIP primers for Sp1? - (reply: 2)
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house-keeping primers for Cos7 cells - (reply: 4)
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increased primer dimer with template - (reply: 2)
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designing the sequencing primer - (reply: 2)
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How long should the DNA fragment be amplified by the two-step PCR? - (reply: 8)
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free software to examine if two primers will make dimers - (reply: 3)
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primer efficiency in real time PCR - need for a method explanasion (reply: 1)
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Mutagenic PCR unsuccessful :( - pls help.... (reply: 7)
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PCR High GC content - PCR High GC content (reply: 11)
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Testing primers - (reply: 3)
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PCR, contamination or not - (reply: 1)
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Me again...on type of polymerase and REs I should use... - (reply: 6)
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design of PRC primers of full ORF - (reply: 3)
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RT-PCR with an old DNaseI? - (reply: 3)
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Two round MSP with the same primer - (reply: 1)
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OD260 and free dNTP - (reply: 3)
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faint pcr bands to some, intense to some - (reply: 5)
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primer dimers - (reply: 4)
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Designing a Primer within an exon - Consesus required - (reply: 2)
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Nested primer PCR - (reply: 5)
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Contamination/no amplification in MSAP-PCR - (reply: 3)
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recommended pcr kits? - (reply: 8)
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No bands at all in gel for PCR products - (reply: 5)
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positive control for RT PCR - (reply: 2)
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Finding PCR Limiting Reagent - (reply: 5)
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Require help with Semi- quantitative PCR protocol - (reply: 10)
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problem wiht long pcr fragment - (reply: 2)
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Old telomerase - PCR elisa kit - can it work? - (reply: 2)
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difference between primer extension and RACE - (reply: 6)
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Amplifying products of different lengths - (reply: 2)
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Is RealTime PCR data enough for Telomerase activity? - (reply: 4)
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Taq PCR and A-tailing - (reply: 2)
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No insert for cloning PCR product into expression vector - (reply: 5)
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using gelatin for PCR - gelatin for PCR (reply: 3)
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designing QRT-PCR Primers - (reply: 11)
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Primer - (reply: 1)
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multiplex PCR - (reply: 4)
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Best way to purify PCR product for sequencing - (reply: 2)
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How can I get the 4.5kb Human typeI procollagen alpha1 chain cDNA Via RT-PCR fr - Seeking Help (reply: 14)
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OCT medium and real time pcr - (reply: 2)
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PCR Smear - (reply: 2)
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amplification fails to reach log linear phase - (reply: 1)
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More RT PCR questions: - can I amplify "everything?" (reply: 2)
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PCR off midiprep - problem with downstream reactions? (reply: 5)
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Ethidium Bromide vs Sybr Green stain (normal PCR) - (reply: 5)
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How many amplifications can you get with PCR? - (reply: 4)
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PCR master Mix problem...Plz help me out - PCR (reply: 8)
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Im stuck with my PCR for nearly 2 months! - i've no bands!! (reply: 5)
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RT-PCR on plasmid - (reply: 1)
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Digesting PCR products and cleaning up digestions - a few quick questions (reply: 4)
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Optimizing primers for SYBR green qPCR? - Optimizing primers for SYBR green qPCR? (reply: 7)
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Hybridation vs Normal PCR - (reply: 2)
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Detection of Bt gene in Corn Through PCR - High School Science Fair - (reply: 6)
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peculiar PCR inhibition - (reply: 11)
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separation of pcr products of similar sizes in agarose gel - (reply: 1)
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Total cDNA PCR - (reply: 3)
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Can I add additional sodium ion to PCR reaction buffers? - (reply: 5)
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Troubleshooting of basic PCR - (reply: 12)
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PCR product precipitation - (reply: 4)
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High Fidelity DNA Polymerase: how many mutations per every kb of amplified DNA o - (reply: 10)
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Cloning PCR product - double bands or heterozygote (reply: 5)
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no band in PCR ! - (reply: 4)
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virtual PCR - (reply: 3)
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Trouble with standard curves for real-time PCR - (reply: 6)
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Real-time PCR machines for DNA quantitation - (reply: 5)
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Contamination from media (MRS) in PCR - (reply: 1)
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purification by gel? - after a first round of PCR (reply: 2)
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rat 18s rRNA primer - designing primers (reply: 1)
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Does Reverse Transcription have to be done using PCR - (reply: 6)
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Which MSP & BGS primer design tool do you "swear" by? - (reply: 9)
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how to improve the efficiency of my FQ-PCR - I can not get a beautiful amplification curve (reply: 3)
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Which technique is Better: Southern Blotting or PCR?? - (reply: 6)
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PCR of AmpR gene - PCR of Amp gene (reply: 1)
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Condition for amplifying >6k PCR - Long PCR amplification (reply: 12)
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PCR reactions - What condition should I use? (reply: 5)
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False positive for colony PCR - (reply: 3)
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inverse PCR or promoter trapping - (reply: 2)
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Overlap PCR - (reply: 2)
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Taq polymerase - (reply: 5)
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Designing primers for multiplex - BLASTing lots of primers (reply: 3)
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Methylation & PCR - (reply: 1)
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optimization of pcr conditions - (reply: 9)
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TaqMan probes, pcr mix - (reply: 1)
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Why random primers for RT-qPCR - (reply: 1)
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What way would you suggest to clean PCR products? - (reply: 4)
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Real Time PCR for Telomerase - (reply: 4)
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Primer design question - Use of primer 3 (reply: 3)
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Can I make four substitutions (mutagenesis) using PCR at a time? - help me out, pls :) (reply: 7)
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Long PCR for amplification from plasmid - (reply: 5)
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RT-PCR detection limits - (reply: 1)
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PCR after Sonication... - (reply: 10)
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PCR Optimization for 50-100 base transcript - How do I increase yield of small PCR product? (reply: 4)
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PCR trouble - (reply: 16)
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Primer extension - yeast tRNA as a negative control (reply: 3)
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cloning of PCR product - (reply: 1)
-
Dimers and weird bands after Bis-PCR - (reply: 5)
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KOD plus for PCR - (reply: 1)
-
Taq polymerase that can run 100 cycles? - (reply: 12)
-
RT-PCR Primer design - which region? - (reply: 2)
-
primer design for MSP - How many CpG in the primer? (reply: 2)
-
Lower size band in genomic PCR with 300 bp missing - (reply: 12)
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PCR - RFLP of plant cpDNA - Can I use several restriction enzyms together? (reply: 2)
-
PCR amplicon size and contamination - (reply: 4)
-
DNA PCR on blood sample - help-Genomic DNA PCR from clogged blood. (reply: 3)
-
Gelatin for PCR - (reply: 2)
-
question of getting a 75bp PCR product - (reply: 1)
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Question about gel purification of PCR product - (reply: 1)
-
DNA amplification - troubleshooting - (reply: 4)
-
nested PCR - (reply: 3)
-
Cloning using RT-PCR for long fragment of 6kb - (reply: 1)
-
No PCR products in MSP with MethPrimer designed primers - (reply: 2)
-
No PCR product - troubleshooting PCR (reply: 12)
-
Taq polymerase dilution? - (reply: 3)
-
How to use Bst polymerase for PCR? - (reply: 8)
-
help pcr cloning problem - help pcr cloning problem!!!!!1 (reply: 2)
-
PCR stop working - (reply: 2)
-
problems with mix of MSP's primers - (reply: 2)
-
pcr ligation - (reply: 2)
-
[PCR products] - (reply: 1)
-
genomic DNA PCR - RE digestion of gDNA before amplification (reply: 3)
-
real time PCR with sybr green - having problems validating my knock down (reply: 3)
-
shorter unspecific PCR product - (reply: 7)
-
PCR an insert in a vector with wrong product size - (reply: 1)
-
Visualization of pcr product before sequencing - (reply: 5)
-
RNA extraction with TRizol and RT-PCR - (reply: 8)
-
Real-time PCR probe degradation - when do they degrades? (reply: 4)
-
design primer for PCR.. - (reply: 3)
-
question about PCR clone a cDNA - (reply: 9)
-
Amplitaq Gold pcr master mix - Protocol question (reply: 1)
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From MSP primer to gene - how to recalculate original DNA sequence? (reply: 4)
-
realtime pcr validating the results of microarray? - (reply: 7)
-
positive NTC in real time PCR - (reply: 8)
-
gel extraction of pcr products - (reply: 3)
-
Design primer - (reply: 2)
-
PCR for more than 5 kb - (reply: 4)
-
cDNA cloning problem - No product in PCR (reply: 5)
-
MSP primers not working - (reply: 1)
-
Is polymerase slippage related to low fidelity? - DNA polymerase slippage during PCR (reply: 2)
-
Quick cloning question - Purification of PCR fragment (reply: 1)
-
No PCR product after BSP, but dimers - (reply: 5)
-
problems with bisulfite PCR - (reply: 8)
-
real time pcr problem - (reply: 4)
-
extra sequence in primers - (reply: 4)
-
Inactivation of Thermo Sequenase / Taq polymerase - (reply: 1)
-
Amplification problems - (reply: 9)
-
PCR TEST FOR DIAGONISTIC - (reply: 3)
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Sybr RT PCR problem - (reply: 4)
-
Primer Programm for Sequencing - (reply: 3)
-
calculating Tm of primers - (reply: 8)
-
real time PCR trouble - real time PCR trouble (reply: 9)
-
AmpliTaq Gold instead of TaqMan Universal PCR Mix in Real-time? - (reply: 3)
-
Primer extension problem - there are too many bands!! (reply: 1)
-
RT-PCR for large fragment - (reply: 7)
-
real time RT-PCR in bacteria - quantitative PCR (reply: 2)
-
nested PCR after bisulphite - (reply: 3)
-
How to design random primers - (reply: 2)
-
design pcr primers - (reply: 3)
-
PCR amplification of >6Kbp DNA - (reply: 2)
-
RT-PCR problem - negative control (reply: 1)
-
How to store PCR product - (reply: 3)
-
Random genoic amplification for microarray - (reply: 4)
-
PCR primers for Mycoplasma detection? - Publication gives many, which to choose? (reply: 1)
-
Real-time PCR - contamination or not? - (reply: 6)
-
Does it help to add antisense primer first for bisulfite PCR? - (reply: 2)
-
Degenerate PCR troubleshooting - (reply: 3)
-
Amount of DNA template in PCR reaction - (reply: 2)
-
A problem of quantitative PCR - (reply: 2)
-
gDNA PCR - (reply: 2)
-
maximum size for PCR - (reply: 3)
-
primer design problem - (reply: 1)
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Bisulfite treated DNA specific primer set critique? - (reply: 18)
-
changing dNTP -> changing PCR conditions? - (reply: 3)
-
60 bp PCR and primer dimers - (reply: 6)
-
Can I directly digest PCR products? - (reply: 9)
-
faint bands of PCR products - (reply: 5)
-
Real Time PCR optimization - standard curve generation (reply: 3)
-
PCR contamination with human DNA - (reply: 5)
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No product/primer dimers after BSP - (reply: 1)
-
bisulfite modification after pcr - (reply: 2)
-
Primer Express Software - Probe Design (reply: 8)
-
Degenerate PCR troubleshooting - (reply: 9)
-
Primer design:Is it ok to omit extra bases after RE site? - (reply: 4)
-
effect of ethanol and dna concentration in pcr - (reply: 3)
-
Problem in Multiplex PCR - Multiplex PCR (reply: 3)
-
PCR small framents - (reply: 2)
-
Problems with methylation analysis!!! - Primers crossreaction etc. (reply: 3)
-
real time PCR (inconsistant results) - (reply: 2)
-
Double digestion of PCR product and ligation - (reply: 5)
-
PCR optimization - (reply: 12)
-
The same PCR gives different results?? - PCR (reply: 1)
-
no band obtain after PCR - (reply: 2)
-
Inconsistent RT-PCR results - (reply: 1)
-
Problem with PCR - (reply: 4)
-
Odd curve of Gel purified PCR product - (reply: 5)
-
primers for SoE - (reply: 1)
-
inconsistent PCR - (reply: 7)
-
Trouble with Inverse PCR - (reply: 8)
-
RAPD PCR help - (reply: 2)
-
multiple band on PCR - (reply: 5)
-
What is the role for gelatin in PCR buffer - (reply: 1)
-
PCR enhancer - (reply: 5)
-
PCR amplifying 50 bp DNA fragment - (reply: 2)
-
Discussion: ChIP PCR control - (reply: 12)
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Help: Question on PCR Cleaning - PCR Cleaning Problem (reply: 3)
-
designing flanking primers around msp primers - (reply: 1)
-
Primer for BSP - (reply: 1)
-
Help: (PCR) Increase template, but NO Increase in product - (reply: 5)
-
BSP cycles and primers - Is it OK to use the same primer set but with more (reply: 6)
-
PCR purification basics? - (reply: 6)
-
primer hairpins and self complementation - online primer checker.. (reply: 2)
-
No PCR products with the ChIP DNA - (reply: 5)
-
Problem amplifying 3 kp fragment from a plasmid - (reply: 4)
-
primer does not bind - help (reply: 2)
-
PCR problems - problems (reply: 2)
-
reconstitute primer - (reply: 4)
-
PCR mix storage - (reply: 1)
-
RT-PCR scale-down makes more sensitive? - (reply: 3)
-
Troubleshooting problem in PCR for bisulfite Treated DNA - (reply: 1)
-
Purification of short PCR product - (reply: 4)
-
No PCR product after bisulfite treatment :( - (reply: 3)
-
PCR Supermix vs Roche - (reply: 3)
-
cloning problem - sticky end cloning with PCR insert - (reply: 3)
-
SOS call: ChIP assay in Huh7 cells - How many cells? And primer position? (reply: 3)
-
Online primer design - (reply: 7)
-
PCR contamination by recombination - (reply: 1)
-
DNase1 problem in PCR - (reply: 6)
-
RT-PCR inconsistent primer efficiencies - RT-PCR (reply: 3)
-
Real-time PCR questions (Mx3000P) - Need some help with interpretation (reply: 7)
-
T4 DNA poymerase - T4 DNA polymerase (reply: 5)
-
TOPO XL cloning with 7.5kb PCR product - troubleshooting help (reply: 1)
-
Unmethylated primer control - (reply: 4)
-
PCR MUTAGENESIS PROBLEM - SiteDirected Mutagenesis - Problem (reply: 3)
-
Cloning large pcr product - efficiency (reply: 2)
-
help me to choose a high fidelity taq polymerase - (reply: 6)
-
how much total RNA do you use for RT-PCR - (reply: 6)
-
One Step RT-PCR cloning problem - (reply: 2)
-
Extremely PCR scale down - (reply: 4)
-
Manipulation with PCR components - Laminar, PCR box? (reply: 3)
-
mastermix for Real-time PCR - (reply: 2)
-
Real time PCR - small peaks in the melt curve - (reply: 5)
-
PCR from genomic DNA - (reply: 1)
-
storage of taq polymerase - (reply: 4)
-
PCR on Leishmania DNA - (reply: 1)
-
is it effective to use a primer of SD rat to Wistar rat in PCR - help (reply: 2)
-
Buffers for storing and diluting of dNTP - (reply: 3)
-
What kind of statistic methods? - RT-PCR (reply: 2)
-
Help a first time cloner with PCR! - First time cloning (reply: 5)
-
Custom Primers - (reply: 2)
-
Primers for RT reaction - (reply: 6)
-
PCR interference? - (reply: 2)
-
Real Time PCR - Relative Quantitation - Choice of calibrator and calculations (reply: 1)
-
Primer Tm - How low can you go? - (reply: 3)
-
PCR product size with a Roche Lightcycler? - (reply: 1)
-
How to prepare primer solution - (reply: 7)
-
Primers design: how to check for mispriming? - (reply: 2)
-
Internal Control RNA & RT-PCR - (reply: 1)
-
PCR from genomic DNA - (reply: 6)
-
Methylated-Specific PCR - (reply: 6)
-
standard curves - real time pcr (reply: 3)
-
primer storage - (reply: 7)
-
EDTA - real time PCR (reply: 3)
-
Cloning and PCR Problems - (reply: 1)
-
Pls check my bisulphite sequencing primers - (reply: 12)
-
rt-PCR false postitives - (reply: 2)
-
Help: Check my MSP primers - is my MSP primer correct??? (reply: 1)
-
Verifying the microarray - real time PCR (reply: 1)
-
How to setup control for bisulfite sequencing PCR - (reply: 2)
-
RT-PCR some questions - (reply: 2)
-
Bad Primer - (reply: 2)
-
Cloning of sequence with PCR added sites - BstBI and BclI (reply: 2)
-
PCR problems - (reply: 3)
-
long range PCR problem - unable to amplify 12 kb fragment (reply: 4)
-
delta delta Ct method - Real time PCR (reply: 4)
-
first strand or double strand cDNA before PCR: RT-qPCR - (reply: 3)
-
Reverse-transcriptase PCR troubleshoot HELP - (reply: 13)
-
reducing primer dimer - (reply: 1)
-
PCR troubleshooting - Primers (reply: 3)
-
PCR problem amplifying 4 kb DNA - (reply: 5)
-
Calculating correct melting temperature for primers - (reply: 2)
-
primer melting temperature - (reply: 2)
-
How can I add sequences to DNA using PCR? - (reply: 1)
-
Bisulfite Sequencing Primer Design - (reply: 3)
-
end of primer - (reply: 2)
-
degenerate primer desgining - degenerate primer desgining (reply: 5)
-
T/A cloning of cDNA? - PGEM-T vs pCR 2.1 T/A TOPO? (reply: 3)
-
Reamplification of RT-PCR product - (reply: 2)
-
PCR primer dimer? - (reply: 7)
-
checking primer - checking primer (reply: 5)
-
How many times for a run -real time pcr - (reply: 1)
-
PCR primer Tm and concentration question - (reply: 3)
-
How to avoid secondary structure in primer - (reply: 2)
-
PCR reamplifying problem - (reply: 5)
-
subcloning of PCR product, please help! - subcloning problems (reply: 12)
-
cloning primer orientation - orientation and complement of primers in a cloning (reply: 3)
-
Random hexamer vs oligo dT vs gene specific primer for RT - which do you use most? (reply: 5)
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primer design - checking off-target site - (reply: 5)
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real-time PCR - (reply: 5)
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NAC (No Amplification Control) - (reply: 2)
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Realtime PCR standard curves - (reply: 8)
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What is the distance between a forward and reverse primer - (reply: 1)
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Real time PCR supermix - (reply: 4)
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differents results in PCR and sequencing!! - (reply: 3)
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PCR contamination mystery - (reply: 2)
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Does residual ethanol in DNA inhibit PCR? - ? (reply: 1)
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Real-time PCR amplification curve up and down - (reply: 3)
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Resuspend probe in real time pcr - (reply: 1)
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Which RT primer is better for qPCR - (reply: 2)
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background signal-real time pcr - (reply: 1)
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HEPA filter - and PCR contamination (reply: 1)
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quencher choice in real time pcr - (reply: 2)
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Problem with amplifying DNA from FTA cards - Is there a special trick involved? (reply: 1)
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PCR; Perhaps someone can explain? - PCR; Primer (reply: 3)
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Why different amounts of forward and reverese primers in RT-QPCR - (reply: 2)
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Degenerate primers - (reply: 1)
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primer optimization - (reply: 1)
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Mx 3000 machine-real time pcr - (reply: 1)
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PCR on plasmids? - (reply: 2)
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PCR with T7 promoter/T7 terminator - (reply: 5)
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Pfx PCR problems - (reply: 1)
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primers for Q-PCR - (reply: 2)
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Storage of RT-PCR products - (reply: 2)
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Detecting 12 nt differences in a 600+ bp pcr product - (reply: 2)
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PCR of a large DNA fragment - (reply: 3)
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multiplex PCR - template and primer concentration (reply: 2)
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Pipetting on ice - during PCR (reply: 5)
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PCR contamination? - (reply: 3)
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Sometimes i get bands, sometimes i get nothing for my PCR - Strange PCR Results (reply: 1)
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Primers and templates - Primer and template concentrations (reply: 2)
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Multiplex PCR troubleshooting - (reply: 6)
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PCR inhibition - (reply: 1)
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Real Time qPCR - qPCR SYBR greenI primer design (reply: 5)
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PCR product on gel as smear - DNA isolated from paraffin blocks why smear? (reply: 1)
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Primers for species identification - Know any good? (reply: 6)
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melt curves for SYBR Green real-time PCR driving me nuts!! - melt curves real-time PCR (reply: 6)
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Genotype ratio with quantitative PCR - (reply: 1)
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The perfect number of CpGs in MSP primer - (reply: 8)
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can't get rid of DNA contamination even with DNase for RT-PCR - (reply: 3)
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Primer Express 2.0 - crashes (reply: 1)
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PCR master mix or super mix - PCR technique (reply: 1)
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relative DNA quantification from PCR - calculation of band intensity from PCR (reply: 2)
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PCR screeing for positive transormation - (reply: 1)
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real-time RT-PCR one cell - (reply: 2)
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Contamination in PCR cloning - (reply: 3)
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Primers - (reply: 1)
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PCR fragment analysis - please help! - PCR fragment analysis - please help! (reply: 2)
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Doublet after real time PCR! - (reply: 3)
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Hot start PCR - (reply: 6)
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dNTP calculation - (reply: 5)
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mutilple bands after RT-PCR - (reply: 2)
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Random primers-real time PCR - (reply: 1)
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How to measure the concentration of primers? - (reply: 2)
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detection of transgene by PCR - (reply: 1)
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Probes or primers that span introns - (reply: 6)
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Tm for my PCR product (not Tm for the primers!) - (reply: 3)
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Problem with second PCR - 1st PCR product and 2nd PCR product are different (reply: 1)
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Primer3 - (reply: 1)
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Cloning a large PCR product - trouble cloning large DNA (reply: 3)
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double sized PCR product from cloned cDNA - (reply: 6)
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real-time pcr plasmid standards - (reply: 4)
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RT-PCR and RE cut site-will this work? - (reply: 3)
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How much of the starting amounts for Real time PCR? - (reply: 1)
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PCR of plasmid miniprep from Agrobacterium - Can't get PCR product out of plasmid miniprep (reply: 1)
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PCR parameters - (reply: 2)
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what primers specific for B.stearothermophilus?Help pls. - (reply: 5)
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Unequal amplification efficiency of heat blocks - (reply: 4)
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Can Taq polymerase be left at room temperature for a long time - (reply: 4)
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PCR colony screening - (reply: 9)
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PCR off of Genomic DNA problems! - -why is my gene without introns showing up?- (reply: 3)
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help regarding primers reconstitution - (reply: 4)
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problem with my PCR - primer dimer. - (reply: 1)
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PCR - Long PCR with short primers (reply: 1)
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invitrogen Superscript one step RT PCR kit - Efficiency of kit (reply: 4)
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Calculating Tm of a PCR product? - (reply: 6)
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PCR techniques (help me) - (reply: 5)
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Sequencing of PCR products - (reply: 5)
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quantitation of PCR bands - (reply: 1)
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a Takara TA taq DNA polymerase protocol - (reply: 1)
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Can BSA help PCR? - (reply: 3)
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how long a primer should I use? - (reply: 1)
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TA cloning with ABgene's extensor HiFi polymerase - (reply: 1)
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problem with PCR --using fragment as template - (reply: 12)
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PCR scaling up doesn't work - (reply: 7)
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real time PCR kit components - (reply: 2)
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Screening of TA cloning by T7/Sp6 PCR possible? - (reply: 2)
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identifying exon and intron for primer design - (reply: 2)
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Can I PCR amplify a ligation product directly - (reply: 3)
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PCR Genomic DNA - PCR Genomic DNA (reply: 1)
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difficulty about cloning 3.5kb PCR product - (reply: 1)
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PCR question - (reply: 3)
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what is the "tailed primer and taq primer"? - (reply: 2)
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Real Time PCR and melting curve - (reply: 2)
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PCR to the PCR!! - (reply: 6)
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threshold for real time PCR - (reply: 1)
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contamination in real-time PCR - (reply: 32)
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TA cloning with short PCR products - use of TA cloning kit (reply: 4)
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Ligation of PCR products - (reply: 1)
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How do you prepare PCR stock solution to minimize pipetting - (reply: 37)
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How do you mix PCR reactions - swish, flick or nothing? - (reply: 44)
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multiplex PCR for 9 exons - (reply: 5)
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Promoter Cloning - PCR amplification of a promoter and cloning (reply: 1)
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Shopping for real-time PCR thermal cyclers - iCycleriQ real-time system? (reply: 1)
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PCR an insert in a vector with wrong product size - I can not amplify my fragment with a normal PCR (reply: 8)
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tRNA and Real time RT-PCR - (reply: 1)
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Problem with TA PCR cloning - no insert in white colonies - (reply: 12)
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Designing methylation primers on long CpG island - (reply: 14)
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Difficutly go separate product from primer dimers - Methylation specific PCR (reply: 1)
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3 bands on RT-PCR - (reply: 4)
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PCR product wrong size (too high) - PCR (reply: 2)
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DNaseI have affect with RT-PCR or not - (reply: 3)
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PCR help - (reply: 5)
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RT- PCR? - (reply: 2)
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ABI7000 + SYBR GREEN I - quantitative PCR (reply: 4)
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real time PCR primer for methylation - (reply: 2)
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designing gene-specific primer for cDNA synthesis - (reply: 5)
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Determine the RNA concentraiton for linear PCR - (reply: 1)
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Purification of small (100bp) PCR products - (reply: 7)
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contamination in real-time pcr negative control - (reply: 12)
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Primer design for unknown gene - (reply: 4)
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TOPO TA pCR 2.1 cloning - (reply: 1)
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How to design primers for CpG, CpNpG, CpHpH methylation - Bisulfite Sequencing PCR (reply: 2)
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Real-time PCR problems - (reply: 3)
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Designing primers from amino acid sequence - cloning problem (reply: 3)
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software to find restriction site and TM for primer - (reply: 7)
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RT-PCR for an intronless gene - (reply: 6)
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Large scale PCR to get milligram of DNA - (reply: 6)
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PCR woes - intermittent empty lanes (reply: 6)
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real-time PCR/ABI Prism 7700 - Std curve programming (reply: 1)
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Extrremely bright bands in the WELLs of PCR agarose gel - Bright and sharp bands in the PCR gel well (reply: 9)
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PCR problem: DISTINCT bands far shorter than target! - (reply: 3)
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Real-time PCR and high Ct value - (reply: 1)
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genotyping transgenic mice with PCR - (reply: 1)
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High fidelity RT-PCR enzymes - looking for choices... (reply: 5)
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Failed to amplify a 2.1 kb PCR product - (reply: 3)
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Reuse of PCR purification column - (reply: 1)
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About PfuTurbo® DNA Polymerase and Pfu DNA Polymerase - (reply: 1)
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Problem with DNase treatment of RNA for RT-PCR - (reply: 1)
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realtime RT-PCR/internal control - (reply: 3)
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PCR and electrophoresis - help finding missing bands! (reply: 3)
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PCR LABORATORY - to avoid contaminations... (reply: 1)
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sense/antisense specific pcr - design of sense/antisense specific pcr primers (reply: 1)
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PCR contamination - (reply: 1)
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Problem with genomic DNA amplification - (reply: 7)
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PCR low amplification - (reply: 2)
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Realtime RT-PCR problem - no product - (reply: 6)
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RT-PCR gone bad - (reply: 4)
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product size for real-time PCR primer - (reply: 3)
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Extraction of adenovirus DNA from cell culture for PCR - protocol (reply: 2)
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RT-PCR - a lot of wrong size fragments. - (reply: 2)
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Which vector for cloning big PCR fragments? - (reply: 3)
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Efficiency Real-Time PCR - Real-time PCR (reply: 3)
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microsatellite PCR from poor quality/trace amounts of DNA - (reply: 3)
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how to produce a high-quality cDNA template for RT-PCR - produce a high-quality cDNA template (reply: 4)
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Asymmetric PCR for generation of single stranded DNA - (reply: 5)
-
PCR Ligation cloning - (reply: 2)
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GC content of PCR primers - (reply: 3)
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real time PCR primers - (reply: 2)
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influence of MgCl2 in PCR - (reply: 7)
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Colony PCR for clone screen - Colony PCR before sending sequence (reply: 4)
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RT-PCR - (reply: 1)
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mC not in CpG? Primer selection - (reply: 1)
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cpgware primer design, does it work - (reply: 4)
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TOPO-TA Cloning PCR product - Is amplicilin selection engough? (reply: 4)
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RT-PCR - 2 kb fragment in RT-PCR (reply: 2)
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PCR does not work - what is the problem? (reply: 2)
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Who will give me a software to design primer for PCR? - (reply: 3)
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old degraded samples. DNA extraction & PCR - (reply: 3)
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No PCR Product for Sequencing - (reply: 5)
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PCR Primer Design with restriction sites - (reply: 1)
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PCR - No bands anymore in well functioning PCR - (reply: 6)
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RT-PCR - (reply: 4)
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problems with PCR long target gene - (reply: 2)
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Hotstart in PCR - (reply: 1)
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No PCR Product - (reply: 2)
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primers with different Tms - PCR amplification using primers with different Tms (reply: 9)
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PCR comparison of gene expression - (reply: 5)
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Reamplification of PCR products - (reply: 2)
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"PCR ghosts" - :wacko: (reply: 2)
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The weirdest PCR ever! - 8kb band in 1min. (reply: 3)
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Sequence input for bisulfite PCR primer design - (reply: 1)
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Primer design for MSP queries - (reply: 3)
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Gradient PCR - (reply: 2)
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Database software to catalogue / archive primers - Database software to catalogue / archive primers (reply: 1)
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PCR Failure..pls help! - (reply: 3)
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PCR with DMSO - (reply: 12)
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Real Time PCR Annealing vs. Melting - Relation of anneal temp rxn to melt temp primer (reply: 2)
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mass balance in PCR - (reply: 3)
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Is there a PCR length limitation after Bisulfite treatment? - (reply: 3)
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PCR blood old samples - (reply: 2)
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RT-PCR with B-cells as template - (reply: 1)
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RT-PCR of different cell lines - (reply: 1)
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PCR for ChIP - PCR for ChIP not working (reply: 3)
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Bisulfite sequencing PCR problem - no products (reply: 3)
-
primer design for bisulphite treated DNA - (reply: 1)
-
methylated genomic DNA PCR - (reply: 1)
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PCR more difficult in methylated CpG region? - (reply: 7)
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primer dimers - what exactly are primer dimers (reply: 2)
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PCR of unknown DNA - PCRing unknown DNA with known linkers (reply: 2)
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primer design: end-point vs. RT - (reply: 1)
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Quantification of PCR using delta-delta Ct method. - Quantification (reply: 1)
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Primers for unmethylated DNA work too well! - (reply: 2)
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ligation of pcr product - (reply: 4)
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software to check the primer dimer - (reply: 3)
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TAQ polymerase is needed - TAQ polymerase for 60 cycles (reply: 1)
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Control for primer extension - (reply: 2)
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How to determine PCR annealing temperature - (reply: 9)
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BSP and MSP primer check - (reply: 2)
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sometimes I get it sometimes I dont - My PCr does not work always (reply: 9)
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Using a big primer in PCR - (reply: 4)
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allele-specific PCR - detection of SNPs by allele-specific amplification (reply: 4)
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No PCR product - Environmental samples (reply: 2)
-
How to remove PCR inhibitors from DNA - (reply: 7)
-
How to get rid of PCR primer dimer - (reply: 65)
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Problem cloning PCR product into double-cut vector - (reply: 3)
-
designed primer more powerful? - (reply: 1)
-
RT-PCR primer design - exon-exon primer design (reply: 5)
-
How to remove DNA for quantitative PCR - (reply: 5)
-
Primer design - PCR for cloning (reply: 6)
-
Long-distance PCR problem - help (reply: 3)
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Promoter amplification.... - (reply: 7)
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PCR Contamination issues - PCR false positives (reply: 106)
-
1-2kb PCR products TOPO cloning troubles - help (reply: 4)
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no template but still got exact size bands???!!! - PCR genotyping problem (reply: 1)
-
RT-PCR for cloning low expressed genes - RT-PCR for cloning low expressed genes (reply: 1)
-
PCR specificity problem - (reply: 5)
-
PCR product for ligation - no PCR product from PCR product (reply: 1)
-
How to qualify PCR productiion concentration? - (reply: 1)
-
availabre primers for MSP - (reply: 1)
-
real time PCR (using Sybr green) - (reply: 1)
-
Strange mobility behavior of PCR products on agarose gel - EB stained vs Gelstar stained (reply: 2)
-
product dimers with GenomeWalker kit - how to deal with them? (reply: 2)
-
PCR or RT-PCR? - (reply: 3)
-
PCR failing - (reply: 18)
-
3' end of forward primer mismatch - (reply: 5)
-
Bisulfite sequencing and PCR issues - (reply: 1)
-
Problem with PCR on difficult template - How to amplify GC-rich region? (reply: 6)
-
PCR Cloning - Please Help - Urgent - Cloning using SalI & BamHI site (reply: 1)
-
DNA quantification - How to quantify my PCR product before sequencing?? (reply: 8)
-
Weak RT-PCR products? - (reply: 1)
-
RACE - specific primers in first strand synthesis (reply: 4)
-
RT PCR - dilution prior to PCR (reply: 2)
-
cloning PCR fragment - PCR fragment is not getting cloned in the vector (reply: 2)
-
qPCR Primer Design and Genomic DNA Amplification - (reply: 1)
-
checking for inserts with colony PCR - (reply: 6)
-
Poor PCR yield - (reply: 4)
-
Primer Designer Online - Pipleline use of designer (reply: 1)
-
Well adding Sybr green in a PCR mix - to detect quicker than by electrophoresis PCR prod (reply: 4)
-
PCR-Check, Screen-Check, MiniPrep - HUH?? - PCR product transformed, grown on AMP, no mini (reply: 2)
-
does anyone know real-time methyaltion pcr? - (reply: 1)
-
Cloning a long PCR product - (reply: 2)
-
Problem in PCR cloning - (reply: 7)
-
If the primer is dimer,it's ok? - (reply: 5)
-
methylation primers - problems with primers (reply: 1)
-
Troubleshoot PCR smear problem - all I got was smear!! (reply: 71)
-
degenerate PCR - (reply: 2)
-
cloning size is not correct - 2 bands on the PCR product (reply: 2)
-
PCR amplification - PCR amplification (reply: 6)
-
Multiplex PCR primer designing - (reply: 4)
-
Smear after second PCR - (reply: 2)
-
still more about cloning PCR products - (reply: 9)
-
single cell PCR - (reply: 8)
-
Annealing temperature for PCR - (reply: 3)
-
Invitrogen platinum pfx enzyme not so fantastic - problems with pcr product gel migration (reply: 1)
-
Genomic DNA amplification - (reply: 4)
-
PCR works first time, then not! - (reply: 1)
-
RT-PCR, why two PCR steps? - two PCRs after reverse transcription?? (reply: 2)
-
total rna extraction from whole blood - for rt pcr (reply: 3)
-
PCR is6110 Tuberculosis - Non specific amplification (reply: 2)
-
PCR from BAC - (reply: 1)
-
Bisulfite modification kits and PCR - (reply: 5)
-
Trouble shooting RT-PCR - (reply: 4)
-
Transformation and PCR questions - (reply: 2)
-
Advice for buying PCR workstation - (reply: 1)
-
PCR contamination in negative control - (reply: 3)
-
RNA isolation from mouse blood - RNA for RT-PCR (reply: 1)
-
PCR Cloning - primer design and CpG methylation (reply: 4)
-
96 Well PCR clean up - Looking for a reliable product (reply: 3)
-
cloning from PCR - (reply: 25)
-
PCR cloning - PCR cloning (reply: 2)
-
sowing pcr? - (reply: 5)
-
real-time PCR - How to design primers (reply: 2)
-
How to identify plasmid - using enzyme and PCR or other? (reply: 2)
-
Which gene is the best internal control for RT-PCR - (reply: 5)
-
BiPolar Clamps on PCR primers for TGGE - (reply: 1)
-
PCR primers - PCR primers for RT-PCR (reply: 1)
-
multiplex primers - (reply: 6)
-
Real Time PCR problem - different dilutions have the same Ct - (reply: 6)
-
Bisulfite PCR: Smear - Can't amplify a certain sequence (reply: 4)
-
RT-PCR;Northern-blotting - internal standard (reply: 4)
-
PCR product sequencing BD v3.1 - Help in removal of residues (reply: 1)
-
Primers: advice? - (reply: 1)
-
RNA and DNA extraction and PCR control - (reply: 1)
-
correct bands in RT-PCR negative control - (reply: 14)
-
About Q-PCR(real-time PCR) - COMPARE (reply: 1)
-
fusion pcr - (reply: 1)
-
dissociation curve of real time pcr products - 2 different peaks in dissociation curve (reply: 2)
-
PCR product purification - (reply: 58)
-
parse primer3 output - (reply: 3)
-
primer3 - select primer in 3' end (reply: 3)
-
bisulfite pcr primers - (reply: 1)
-
bisulfite modification of dna for pcr - (reply: 1)
-
The PCR Suite - a set of new primer design tools - (reply: 1)
-
methylation specific PCR (MSP) - reproducibilty? (reply: 1)
-
pcr ligation - problems with ligation (reply: 1)
-
PCR - (reply: 1)
-
PCR problem - can not get the target SSR band (reply: 1)
-
RT-PCR, RNA isolation, etc. - (reply: 1)
-
RT-PCR amplification problem - amplification problem (reply: 1)
-
contamination PCR - (reply: 3)
-
PCR problems - (reply: 4)
-
Genomic PCR - (reply: 2)
-
Is there anybody use Taq polymerase of Fermemtas - (reply: 20)
-
multiplex PCR - (reply: 1)
-
Amplification Problem - PCR Failure... (reply: 5)
-
RT-PCR primer design guide - How to check gene structure and design the primer? (reply: 15)
-
LacZ PCR - (reply: 1)
-
about semi-quantity of PCR products on agarose gel - (reply: 2)
-
Fusion PCR Protocol? - (reply: 6)
-
PCR artefacts - (reply: 1)
-
Primer dimers - (reply: 1)
-
PCR Cloning - (reply: 1)
-
RT-PCR 1 step - (reply: 2)
-
does hot lid matter? - PCR problem (reply: 9)
-
PCR and Primers - PCR-no products (reply: 4)
-
Double strand cDNA sysnthesis - Using random primers (reply: 1)
-
AMPLIFYING LONG FRAGMENTS - problems obtaining 3kb fragment (reply: 4)
-
RNA contamination PCR - RNA contamination PCR (reply: 1)
-
Amplification Failure of Unknown Reason - (reply: 1)
-
APOE PCR conditions - RFLP e2, e3, e4? (reply: 5)
-
Ammonium Sulfate PCR buffer - Ammonium Sulfate PCR buffer (reply: 1)
-
degenerate primer - optimizing degenerate primers (reply: 1)
-
Detection in SmartCycler RT-PCR - (reply: 1)
-
Long PCR problem - Product smaller than expected size (reply: 3)
-
Probes for Real-Time PCR - (reply: 3)
-
gDNA contamination in RT-PCR - (reply: 2)
-
DNA Contamination in RNA? - PCR of RNA (reply: 1)
-
reference on PCR using degenerate primers - Help me find the reference (reply: 1)
-
Help! DNA contamination in RNA and RT-PCR. - (reply: 1)
-
simple pcr questions - simple pcr questions (reply: 1)
-
Problems in my Multiplex PCR - (reply: 6)
-
pcr select cdna subtraction - kit from clontech (reply: 1)
-
PCR detection of water-bornebacteria - (reply: 1)
-
Kit for Mycoplasma detection by PCR - (reply: 4)
-
Sequencing PCR products - (reply: 2)
-
Whole Cell PCR from BacteriaProtocols? - (reply: 4)
-
cDNA PCR - Amplifying region using PCR from cDNA library (reply: 1)
-
tomato DNA for PCR template - (reply: 1)
-
tomato DNA for PCR - (reply: 1)
-
Inverse /ligation-mediated PCR - 5'-flanking region amplification (reply: 1)
-
Re: dNTP make up - (reply: 1)
-
Need suggestions for degenerate primers - (reply: 2)
-
My PCR is not work again - (reply: 6)
-
phage PCR - (reply: 1)
-
PCR from parraffin embeded samples - (reply: 2)
-
Primer extension - (reply: 1)
-
Primer design - Primer design for RT-PCR (reply: 1)
-
I am afraid I got wrong Primer from company - (reply: 2)
-
Difficult PCR amplification of 4kb genomic DNA - (reply: 3)
-
long PCR for mtDNA - (reply: 1)
-
Primer contamination - (reply: 2)
-
PCR amplification in negative control - (reply: 1)
-
PCR on cDNA libraries - (reply: 2)
-
sequencing of Pcr product - (reply: 4)
-
Blunting 3' ends with T4 polymerase - (reply: 1)
-
Gene copy number by PCR - (reply: 1)
-
Difference between RNase Protention and RT-PCR - (reply: 1)
-
RT-PCR - (reply: 2)
-
A variation of the usual PCRprotocol needed - (reply: 3)
-
degenerated primer for nested RT PCR - (reply: 5)
-
RNase and PCR - (reply: 1)
-
RT-PCR - (reply: 1)
-
pcr mutagenesis - (reply: 3)
-
questions about degenerate primer PCR - (reply: 2)
-
design a primer - how to determind a specific primer in a complete gonome? (reply: 1)
-
RT-PCR - (reply: 1)
-
dUTP used for PCR - (reply: 6)
-
PCR and Cultures - PCR and Cultures (reply: 1)
-
PCR with cell source - (reply: 1)
-
PCR - (reply: 1)
-
In situ PCR and hybridization in plant - In situ PCR/hybridization protocols (reply: 1)
-
RT PCR - (reply: 1)
-
Difference in RT PCR products when using total RNA or mRNA - (reply: 4)
-
ligation problems - cloning a PCR fragment - into a double-cut vector (reply: 4)
-
PCR mutagenesis - (reply: 1)
-
RT-PCR, help needed - (reply: 2)
-
M13 phage amplification,who canhelp? - (reply: 2)
-
Overlap PCR that will notamplify - (reply: 1)
-
Poor PCR result - (reply: 2)
-
Error-prone PCR - (reply: 1)
-
Rt-PCR help,come in - use RT (reply: 2)
-
Dimers on SDS-PAGE - (reply: 2)
-
PCR or Southern? - (reply: 3)
-
Pcr cloning - how to get a single band (reply: 4)
-
hot start Taq - Taq polymerase (reply: 1)
-
RNA isolation from isolatedislets and RT-PCR - (reply: 1)
-
How to find/check the highly conservative sequence - RT-PCR primers (reply: 2)
-
How to PCR GC-rich inserts - (reply: 2)
-
RT-PCR - (reply: 2)
-
Nested PCR sensitivity - (reply: 3)
-
pcr on genomic dna ( tailsmouse), HELP !!!! - (reply: 2)
-
SOE PCR - (reply: 1)
-
Bioinfomatics (ePCR) - (reply: 1)
-
cloning of pcr product - (reply: 2)
-
About Marker - for PCR (reply: 2)
-
Genomic Boiling Prep for PCR - quick way to obtain PCR template (reply: 2)
-
Trypsin - PCR amplification (reply: 1)
-
making radioactive DNA probesusing PCR - (reply: 1)
-
PCR problem - non specific bands - pcr problem (reply: 8)
-
Scorpion Primers? - Synthese of Scorpion Primer (reply: 1)
-
Poor PCR Results - (reply: 3)
-
problem with Rt-PCR - (reply: 1)
-
ABI377 Sequencing of PCR products - (reply: 1)
-
amplifiable dna from bones - procedure for dna isolation from bones (reply: 4)
-
How to clean agar contamination for colony PCR - (reply: 2)
-
Cloning error prone PCR products - (reply: 1)
-
PCR problems - (reply: 1)
-
genotyping transgenic mice with PCR - (reply: 1)
-
PCR restriction site - (reply: 2)
-
deletion pcr - deletion pcr gene (reply: 3)
-
Single-cell RT-PCR with only ~10-100 Cells - (reply: 2)
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Problems with PCR Purification - When I try to purify my PCR product I lose all of my DNA? (reply: 4)
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C-MYC AND CYCLIN D1 / RT-PCR - (reply: 2)
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Amount of genomic DNA for PCRamplication - (reply: 1)
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a question about RT-PCR - (reply: 1)
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Re: PCR cloning problem - (reply: 1)
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primer purification - search method for primer purifying (reply: 3)
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PCR amplification of the terminal repeat - (reply: 1)
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How to make PCR using the gel solution - (reply: 1)
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primer design tools - primer designing (reply: 28)
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Software for MSP (methylation-specific PCR) primer design - (reply: 3)
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Bioinfomatics (ePCR) - (reply: 9)
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primer design - Deinococcus (reply: 1)