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