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Top : New Forum Archives (2009-): : Molecular-Biology
181. Low A260/230 after gel extraction - (reply: 1)
182. forgotten the kits at room temperature - (reply: 6)
183. Disparity between nanodrop and gel - (reply: 2)
184. tripure rna isolation - (reply: 1)
185. Graphics Software with Scaling - (reply: 1)
186. How to remove inhibitory substances in PCR? - (reply: 2)
187. DNA exraction from parasites - (reply: 1)
188. How to increase protein expression from in vitro transcribed mRNA - (reply: 1)
189. What is the current best site-direct mutagenesis Kits? - (reply: 1)
190. RNA agarose gel electrophoresis came up empty - (reply: 10)
191. high basal levels of fluorescence in flow cytometry - (reply: 2)
192. Tissue Preservation - (reply: 1)
193. Troubleshooting qPCR standards - (reply: 1)
194. troubleshooting stubborn PCR - (reply: 6)
195. Puromycin resistance protein expression and stability - (reply: 5)
196. Why would you use DNase as a control in dot blot assay confirming viroid import? - (reply: 1)
197. tissue homogenization problem - (reply: 5)
198. Top of agarose gel blank? - (reply: 3)
199. Plasmid storage conditions - (reply: 5)
200. Top10 and DH10B need IPTG for induction? - (reply: 1)
201. Cell lysis and DNA quantification - (reply: 1)
202. New (free) plasmid mapping program - (reply: 4)
203. E coli culture cannot grow overnight. - (reply: 11)
204. Problem with in vitro transcription - (reply: 1)
205. excess amount of primers - (reply: 2)
206. Dehydrating and Reconstituting primers - (reply: 15)
207. Trouble with PCR of short sequence - (reply: 3)
208. EtBr decontamination of gel doc system - (reply: 2)
209. RNA Precipitation - (reply: 1)
210. filling the digested vector and insert for blunt end cloning - (reply: 2)