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241. Changing the vector - (reply: 55)
242. The PCR gods are frowning upon me - (reply: 9)
243. Viral RNA in total RNA eluate for transfection - (reply: 1)
244. page electrophoresis - (reply: 2)
245. Low A260/230 after gel extraction - (reply: 1)
246. forgotten the kits at room temperature - (reply: 6)
247. Disparity between nanodrop and gel - (reply: 2)
248. tripure rna isolation - (reply: 1)
249. Graphics Software with Scaling - (reply: 1)
250. How to remove inhibitory substances in PCR? - (reply: 2)
251. DNA exraction from parasites - (reply: 1)
252. How to increase protein expression from in vitro transcribed mRNA - (reply: 1)
253. What is the current best site-direct mutagenesis Kits? - (reply: 1)
254. RNA agarose gel electrophoresis came up empty - (reply: 10)
255. high basal levels of fluorescence in flow cytometry - (reply: 2)
256. Tissue Preservation - (reply: 1)
257. Troubleshooting qPCR standards - (reply: 1)
258. troubleshooting stubborn PCR - (reply: 6)
259. Puromycin resistance protein expression and stability - (reply: 5)
260. Why would you use DNase as a control in dot blot assay confirming viroid import? - (reply: 1)
261. tissue homogenization problem - (reply: 5)
262. Top of agarose gel blank? - (reply: 3)
263. Plasmid storage conditions - (reply: 5)
264. Top10 and DH10B need IPTG for induction? - (reply: 1)
265. Cell lysis and DNA quantification - (reply: 1)
266. New (free) plasmid mapping program - (reply: 4)
267. E coli culture cannot grow overnight. - (reply: 11)
268. Problem with in vitro transcription - (reply: 1)
269. excess amount of primers - (reply: 2)
270. Dehydrating and Reconstituting primers - (reply: 15)
242. The PCR gods are frowning upon me - (reply: 9)
243. Viral RNA in total RNA eluate for transfection - (reply: 1)
244. page electrophoresis - (reply: 2)
245. Low A260/230 after gel extraction - (reply: 1)
246. forgotten the kits at room temperature - (reply: 6)
247. Disparity between nanodrop and gel - (reply: 2)
248. tripure rna isolation - (reply: 1)
249. Graphics Software with Scaling - (reply: 1)
250. How to remove inhibitory substances in PCR? - (reply: 2)
251. DNA exraction from parasites - (reply: 1)
252. How to increase protein expression from in vitro transcribed mRNA - (reply: 1)
253. What is the current best site-direct mutagenesis Kits? - (reply: 1)
254. RNA agarose gel electrophoresis came up empty - (reply: 10)
255. high basal levels of fluorescence in flow cytometry - (reply: 2)
256. Tissue Preservation - (reply: 1)
257. Troubleshooting qPCR standards - (reply: 1)
258. troubleshooting stubborn PCR - (reply: 6)
259. Puromycin resistance protein expression and stability - (reply: 5)
260. Why would you use DNase as a control in dot blot assay confirming viroid import? - (reply: 1)
261. tissue homogenization problem - (reply: 5)
262. Top of agarose gel blank? - (reply: 3)
263. Plasmid storage conditions - (reply: 5)
264. Top10 and DH10B need IPTG for induction? - (reply: 1)
265. Cell lysis and DNA quantification - (reply: 1)
266. New (free) plasmid mapping program - (reply: 4)
267. E coli culture cannot grow overnight. - (reply: 11)
268. Problem with in vitro transcription - (reply: 1)
269. excess amount of primers - (reply: 2)
270. Dehydrating and Reconstituting primers - (reply: 15)