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241. where to get vector overexpressing caveolin-1? - (reply: 2)
242. Colony PCR works but DNA yeild very low after miniprep - (reply: 2)
243. LZRS vector details - (reply: 1)
244. 12.4kb vector 6.7kb insert - (reply: 2)
245. Stable transfection - (reply: 2)
246. Using normal competent cells in electroporation method? - (reply: 1)
247. an effective way to do a yeast colony pcr - (reply: 2)
248. pGEM-T Easy vector contamination - (reply: 2)
249. recover old transformed DH5 - (reply: 1)
250. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
251. oligo(dt) 15 vs random primers - (reply: 3)
252. I need bynary vector pART27 - (reply: 1)
253. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
254. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
255. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
256. cloning into Pgem t easy - (reply: 1)
257. How to get pure protein of a gene - (reply: 3)
258. How to insert genes into chromosome of E. coli - (reply: 1)
259. Gene synthesis - (reply: 2)
260. Pls help me with this plasmid!!! - (reply: 1)
261. Problems with Restriction Digest Results - (reply: 7)
262. Methods of plasmid transformation? only heat shock? - (reply: 1)
263. Digestion - (reply: 2)
264. Digestion of Genomic DNA - (reply: 1)
265. Isolation of a Gene of Interest for Subcloning - (reply: 8)
266. E.coli grow on neg. control - (reply: 1)
267. Transformed cells have many mutations! pET-46 Ek/LIC + sequence verified ins - (reply: 1)
268. Need help troubleshooting digest. - (reply: 1)
269. Competent cells question: JM101 vs DH5alpha - (reply: 2)
270. How to avoid plasmid instability - (reply: 4)
242. Colony PCR works but DNA yeild very low after miniprep - (reply: 2)
243. LZRS vector details - (reply: 1)
244. 12.4kb vector 6.7kb insert - (reply: 2)
245. Stable transfection - (reply: 2)
246. Using normal competent cells in electroporation method? - (reply: 1)
247. an effective way to do a yeast colony pcr - (reply: 2)
248. pGEM-T Easy vector contamination - (reply: 2)
249. recover old transformed DH5 - (reply: 1)
250. NZY+Broth can be replaced by LB Broth in mutagenesis exp - (reply: 2)
251. oligo(dt) 15 vs random primers - (reply: 3)
252. I need bynary vector pART27 - (reply: 1)
253. Plasmid with two similar bacterial ORIs - Can it be transformed into bacteria?? - (reply: 2)
254. Why don't I get the expected entry clones when I use the gateway system?? - (reply: 2)
255. Need help verifying promotor of a PUC19 based plasmid - (reply: 1)
256. cloning into Pgem t easy - (reply: 1)
257. How to get pure protein of a gene - (reply: 3)
258. How to insert genes into chromosome of E. coli - (reply: 1)
259. Gene synthesis - (reply: 2)
260. Pls help me with this plasmid!!! - (reply: 1)
261. Problems with Restriction Digest Results - (reply: 7)
262. Methods of plasmid transformation? only heat shock? - (reply: 1)
263. Digestion - (reply: 2)
264. Digestion of Genomic DNA - (reply: 1)
265. Isolation of a Gene of Interest for Subcloning - (reply: 8)
266. E.coli grow on neg. control - (reply: 1)
267. Transformed cells have many mutations! pET-46 Ek/LIC + sequence verified ins - (reply: 1)
268. Need help troubleshooting digest. - (reply: 1)
269. Competent cells question: JM101 vs DH5alpha - (reply: 2)
270. How to avoid plasmid instability - (reply: 4)