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Molecular-Biology
3211.
can we add the terminaton codon in the 3' primer? -
(reply: 1)
3212.
KpnI and BamHI double digest help -
(reply: 6)
3213.
How many genes in Arabidopsis thaliana ? -
(reply: 2)
3214.
Size of 23s and 16s RNA different -
(reply: 3)
3215.
PCR probes for Southern blot -
(reply: 1)
3216.
Smear in PCR -
(reply: 5)
3217.
PCR amplification -
(reply: 2)
3218.
Maintaining organellar genomes - What's the force?
(reply: 1)
3219.
Site directed mutagenesis - wild type clone
(reply: 4)
3220.
Cloning - intronic sequences needed? -
(reply: 4)
3221.
Specific Specificity! - abt L/D- AAs ,D/L-sugars & all...
(reply: 1)
3222.
Primer dimers?Contaminations? - Unexpected bands!
(reply: 5)
3223.
hybridizazion - southern
(reply: 1)
3224.
reverse primer design with restriction site -
(reply: 6)
3225.
Tissue sample storage -
(reply: 1)
3226.
Denaturing Agarose gel for RNA -
(reply: 10)
3227.
BRAIN RNA EXTRACTION! -
(reply: 3)
3228.
Unstable clones -
(reply: 3)
3229.
how does dsDNA probes work in Northern ? - its a very basic qn but i am confused
(reply: 5)
3230.
glass milk for DNA cleanup? -
(reply: 1)
3231.
Is it obligatory to precipitate DNA from ligation before transformed into E.coli -
(reply: 7)
3232.
southern again - transfert
(reply: 4)
3233.
southern - loading DNA
(reply: 2)
3234.
Expression analysis -
(reply: 1)
3235.
Different RNA sources, Different PCR optimal condition? -
(reply: 5)
3236.
question in 5' RACE and primer extesion -
(reply: 8)
3237.
about Band - genomic DNA of liver of mouse
(reply: 2)
3238.
Smear in Native PAGE -
(reply: 1)
3239.
sequencing through insertions sequences -
(reply: 2)
3240.
PCR contamination - does autoclaving help? -
(reply: 7)
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