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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
211. Need help to identify bands in AGE result - (reply: 3)
212. COLD-PCR (Dissociation Curve) via qPCR - (reply: 4)
213. how to hasten real-time PCR amplifications - (reply: 2)
214. Please please help me with my Phusion PCR. - (reply: 5)
215. Nanodrop vs Picogreen to quantify post-PCR product - (reply: 3)
216. Need no RT control for all genes? - (reply: 1)
217. Different annealing temp between HKG and target gene - (reply: 2)
218. Multiple melt curves for primer in a sample that does not express gene - (reply: 6)
219. help in long pcr - (reply: 1)
220. Reselling a supermix/enzyme in a commercial diagnostic kit - (reply: 2)
221. Small yield of RNA after on column DNAs digestion , Why - (reply: 3)
222. PCR inhibitor in template DNA - (reply: 3)
223. Why when disigning primers for RTPCR, you need to chose a region where introns a - (reply: 1)
224. Problem with Real-time PCR results analysis - (reply: 1)
225. Rotor-Gene 6000 data analysis - (reply: 1)
226. PCR from protozoa DNA - (reply: 3)
227. Ligation-mediated PCR: Vent Polymerase, Why? - (reply: 7)
228. tool for comparing many primers pairs - (reply: 4)
229. PCR that leads to protein synthesis - (reply: 18)
230. Real-time PCR does not work, while the conventional PCR (with same conditions an - (reply: 3)
231. Use of DMSO in General PCR - (reply: 1)
232. PCR product size confusion - (reply: 3)
233. Concentration specification in PCR - (reply: 3)
234. help us understand the run - (reply: 1)
235. Different MOI in comparison experiment - (reply: 3)
236. How to determine the size of gene to amplify? - (reply: 1)
237. Guanidine isothiocyanate in PCR - (reply: 1)
238. Untreated samples negative, how to analyze fold change? - (reply: 1)
239. Primers have worked well but now getting primer dimers? - (reply: 2)
240. I cannot design primers on exon-exon junction - (reply: 2)