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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
241. tool for comparing many primers pairs - (reply: 4)
242. PCR that leads to protein synthesis - (reply: 18)
243. Real-time PCR does not work, while the conventional PCR (with same conditions an - (reply: 3)
244. Use of DMSO in General PCR - (reply: 1)
245. PCR product size confusion - (reply: 3)
246. Concentration specification in PCR - (reply: 3)
247. help us understand the run - (reply: 1)
248. Different MOI in comparison experiment - (reply: 3)
249. How to determine the size of gene to amplify? - (reply: 1)
250. Guanidine isothiocyanate in PCR - (reply: 1)
251. Untreated samples negative, how to analyze fold change? - (reply: 1)
252. Primers have worked well but now getting primer dimers? - (reply: 2)
253. I cannot design primers on exon-exon junction - (reply: 2)
254. DNA Quantification of PCR Products - (reply: 2)
255. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
256. Problem for PCR - (reply: 9)
257. Confused about my CT values - (reply: 1)
258. Designing primers in UTRs - (reply: 1)
259. Multiplex PCR - (reply: 1)
260. primer design@ buy? - (reply: 2)
261. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
262. Dissolving DNA Oligos - (reply: 2)
263. Trouble with overlap extension pcr - (reply: 3)
264. copies per ul to copies per gram tissue - (reply: 2)
265. designing primers( selecting target sequence/amplicon design) - (reply: 3)
266. Question about the RT PCR - (reply: 3)
267. PCR ready mixes with long shelf lives - (reply: 4)
268. Problem with repeatability of the standard curve - (reply: 3)
269. Influenza virus - (reply: 3)
270. Defining standards in qPCR softwares - (reply: 3)