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301. Quick method for DNA extraction using lysis - (reply: 4)
302. Editing out secondary potential ORFs? - (reply: 2)
303. Sterility issues with plasmid reconstitution buffer? - (reply: 3)
304. Heating elution buffer for plasmid prep - (reply: 1)
305. qPCR and miRNA isolation - (reply: 4)
306. Yeast Two Hybrid system - (reply: 7)
307. how much purify protein nedded for IP - (reply: 9)
308. lyophilized protein dilution - (reply: 6)
309. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
310. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
311. finding a reference for a formula - (reply: 2)
312. CHO-K1 transfection problem - (reply: 2)
313. Not Template Control Contamination - (reply: 7)
314. Mesenchymal stem cells Expressing BDNF - (reply: 5)
315. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
316. How to do a primer dilution - (reply: 10)
317. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
318. gDNA still presents even after DNase treatment - (reply: 6)
319. help interpreting this data - (reply: 2)
320. 293t transfected with prtTA inducible vex - (reply: 5)
321. RNA contamination in plasmid extracted - (reply: 1)
322. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
323. PCR and sequencing of genomic DNA - (reply: 5)
324. Virus sample - (reply: 3)
325. NESTED PCR - (reply: 6)
326. Electroporation query - (reply: 7)
327. Failed cloning - different readings - (reply: 10)
328. mRNA copies of each gene under different promoters - (reply: 1)
329. Purified DNA fragments are bigger than unpurified - (reply: 2)
330. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)
302. Editing out secondary potential ORFs? - (reply: 2)
303. Sterility issues with plasmid reconstitution buffer? - (reply: 3)
304. Heating elution buffer for plasmid prep - (reply: 1)
305. qPCR and miRNA isolation - (reply: 4)
306. Yeast Two Hybrid system - (reply: 7)
307. how much purify protein nedded for IP - (reply: 9)
308. lyophilized protein dilution - (reply: 6)
309. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
310. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
311. finding a reference for a formula - (reply: 2)
312. CHO-K1 transfection problem - (reply: 2)
313. Not Template Control Contamination - (reply: 7)
314. Mesenchymal stem cells Expressing BDNF - (reply: 5)
315. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
316. How to do a primer dilution - (reply: 10)
317. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
318. gDNA still presents even after DNase treatment - (reply: 6)
319. help interpreting this data - (reply: 2)
320. 293t transfected with prtTA inducible vex - (reply: 5)
321. RNA contamination in plasmid extracted - (reply: 1)
322. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
323. PCR and sequencing of genomic DNA - (reply: 5)
324. Virus sample - (reply: 3)
325. NESTED PCR - (reply: 6)
326. Electroporation query - (reply: 7)
327. Failed cloning - different readings - (reply: 10)
328. mRNA copies of each gene under different promoters - (reply: 1)
329. Purified DNA fragments are bigger than unpurified - (reply: 2)
330. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)