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241. Quick method for DNA extraction using lysis - (reply: 4)
242. Editing out secondary potential ORFs? - (reply: 2)
243. Sterility issues with plasmid reconstitution buffer? - (reply: 3)
244. Heating elution buffer for plasmid prep - (reply: 1)
245. qPCR and miRNA isolation - (reply: 4)
246. Yeast Two Hybrid system - (reply: 7)
247. how much purify protein nedded for IP - (reply: 9)
248. lyophilized protein dilution - (reply: 6)
249. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
250. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
251. finding a reference for a formula - (reply: 2)
252. CHO-K1 transfection problem - (reply: 2)
253. Not Template Control Contamination - (reply: 7)
254. Mesenchymal stem cells Expressing BDNF - (reply: 5)
255. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
256. How to do a primer dilution - (reply: 10)
257. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
258. gDNA still presents even after DNase treatment - (reply: 6)
259. help interpreting this data - (reply: 2)
260. 293t transfected with prtTA inducible vex - (reply: 5)
261. RNA contamination in plasmid extracted - (reply: 1)
262. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
263. PCR and sequencing of genomic DNA - (reply: 5)
264. Virus sample - (reply: 3)
265. NESTED PCR - (reply: 6)
266. Electroporation query - (reply: 7)
267. Failed cloning - different readings - (reply: 10)
268. mRNA copies of each gene under different promoters - (reply: 1)
269. Purified DNA fragments are bigger than unpurified - (reply: 2)
270. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)
242. Editing out secondary potential ORFs? - (reply: 2)
243. Sterility issues with plasmid reconstitution buffer? - (reply: 3)
244. Heating elution buffer for plasmid prep - (reply: 1)
245. qPCR and miRNA isolation - (reply: 4)
246. Yeast Two Hybrid system - (reply: 7)
247. how much purify protein nedded for IP - (reply: 9)
248. lyophilized protein dilution - (reply: 6)
249. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
250. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
251. finding a reference for a formula - (reply: 2)
252. CHO-K1 transfection problem - (reply: 2)
253. Not Template Control Contamination - (reply: 7)
254. Mesenchymal stem cells Expressing BDNF - (reply: 5)
255. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
256. How to do a primer dilution - (reply: 10)
257. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
258. gDNA still presents even after DNase treatment - (reply: 6)
259. help interpreting this data - (reply: 2)
260. 293t transfected with prtTA inducible vex - (reply: 5)
261. RNA contamination in plasmid extracted - (reply: 1)
262. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
263. PCR and sequencing of genomic DNA - (reply: 5)
264. Virus sample - (reply: 3)
265. NESTED PCR - (reply: 6)
266. Electroporation query - (reply: 7)
267. Failed cloning - different readings - (reply: 10)
268. mRNA copies of each gene under different promoters - (reply: 1)
269. Purified DNA fragments are bigger than unpurified - (reply: 2)
270. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)