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Top : New Forum Archives (2009-): : Molecular-Biology
241. how much purify protein nedded for IP - (reply: 9)
242. lyophilized protein dilution - (reply: 6)
243. Do homologous arms need to overlap right at the DSB for knock-in - (reply: 1)
244. Is it possible quantify dsDNA pre-sequencing with a kit in stepone plus qpcr - (reply: 2)
245. finding a reference for a formula - (reply: 2)
246. CHO-K1 transfection problem - (reply: 2)
247. Not Template Control Contamination - (reply: 7)
248. Mesenchymal stem cells Expressing BDNF - (reply: 5)
249. Problem with Site-directed mutagenesis of a 9 kb template with high GC content ( - (reply: 3)
250. How to do a primer dilution - (reply: 10)
251. Can I use an EtBr stained PAGE gel for northern blot? - (reply: 2)
252. gDNA still presents even after DNase treatment - (reply: 6)
253. help interpreting this data - (reply: 2)
254. 293t transfected with prtTA inducible vex - (reply: 5)
255. RNA contamination in plasmid extracted - (reply: 1)
256. 0.2 vs 0.45um filter for clearing retro- or lentiviral supernatant? - (reply: 2)
257. PCR and sequencing of genomic DNA - (reply: 5)
258. Virus sample - (reply: 3)
259. NESTED PCR - (reply: 6)
260. Electroporation query - (reply: 7)
261. Failed cloning - different readings - (reply: 10)
262. mRNA copies of each gene under different promoters - (reply: 1)
263. Purified DNA fragments are bigger than unpurified - (reply: 2)
264. Phoenix Amphoteric cell line to package lentivirus? - (reply: 6)
265. Digestion necessary after PCR? - (reply: 9)
266. Merodiploids on sucrose plates? - (reply: 1)
267. Inverse PCR product selection - (reply: 2)
268. Dead cells after transfection - (reply: 9)
269. Review of antisense chemistries - (reply: 1)
270. DNA extraction from endive (low yield + peak at 220 nm) - (reply: 4)