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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
211. Need no RT control for all genes? - (reply: 1)
212. Different annealing temp between HKG and target gene - (reply: 2)
213. Multiple melt curves for primer in a sample that does not express gene - (reply: 6)
214. help in long pcr - (reply: 1)
215. Reselling a supermix/enzyme in a commercial diagnostic kit - (reply: 2)
216. Small yield of RNA after on column DNAs digestion , Why - (reply: 3)
217. PCR inhibitor in template DNA - (reply: 3)
218. Why when disigning primers for RTPCR, you need to chose a region where introns a - (reply: 1)
219. Problem with Real-time PCR results analysis - (reply: 1)
220. Rotor-Gene 6000 data analysis - (reply: 1)
221. PCR from protozoa DNA - (reply: 3)
222. Ligation-mediated PCR: Vent Polymerase, Why? - (reply: 7)
223. tool for comparing many primers pairs - (reply: 4)
224. PCR that leads to protein synthesis - (reply: 18)
225. Real-time PCR does not work, while the conventional PCR (with same conditions an - (reply: 3)
226. Use of DMSO in General PCR - (reply: 1)
227. PCR product size confusion - (reply: 3)
228. Concentration specification in PCR - (reply: 3)
229. help us understand the run - (reply: 1)
230. Different MOI in comparison experiment - (reply: 3)
231. How to determine the size of gene to amplify? - (reply: 1)
232. Guanidine isothiocyanate in PCR - (reply: 1)
233. Untreated samples negative, how to analyze fold change? - (reply: 1)
234. Primers have worked well but now getting primer dimers? - (reply: 2)
235. I cannot design primers on exon-exon junction - (reply: 2)
236. DNA Quantification of PCR Products - (reply: 2)
237. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
238. Problem for PCR - (reply: 9)
239. Confused about my CT values - (reply: 1)
240. Designing primers in UTRs - (reply: 1)