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Top : New Forum Archives (2009-): : Molecular-Biology
181. Antisense probe as negative control for in situ hybridization - (reply: 1)
182. Changing the vector - (reply: 55)
183. The PCR gods are frowning upon me - (reply: 9)
184. Viral RNA in total RNA eluate for transfection - (reply: 1)
185. page electrophoresis - (reply: 2)
186. Low A260/230 after gel extraction - (reply: 1)
187. forgotten the kits at room temperature - (reply: 6)
188. Disparity between nanodrop and gel - (reply: 2)
189. tripure rna isolation - (reply: 1)
190. Graphics Software with Scaling - (reply: 1)
191. How to remove inhibitory substances in PCR? - (reply: 2)
192. DNA exraction from parasites - (reply: 1)
193. How to increase protein expression from in vitro transcribed mRNA - (reply: 1)
194. What is the current best site-direct mutagenesis Kits? - (reply: 1)
195. RNA agarose gel electrophoresis came up empty - (reply: 10)
196. high basal levels of fluorescence in flow cytometry - (reply: 2)
197. Tissue Preservation - (reply: 1)
198. Troubleshooting qPCR standards - (reply: 1)
199. troubleshooting stubborn PCR - (reply: 6)
200. Puromycin resistance protein expression and stability - (reply: 5)
201. Why would you use DNase as a control in dot blot assay confirming viroid import? - (reply: 1)
202. tissue homogenization problem - (reply: 5)
203. Top of agarose gel blank? - (reply: 3)
204. Plasmid storage conditions - (reply: 5)
205. Top10 and DH10B need IPTG for induction? - (reply: 1)
206. Cell lysis and DNA quantification - (reply: 1)
207. New (free) plasmid mapping program - (reply: 4)
208. E coli culture cannot grow overnight. - (reply: 11)
209. Problem with in vitro transcription - (reply: 1)
210. excess amount of primers - (reply: 2)