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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
241. PCR product size confusion - (reply: 3)
242. Concentration specification in PCR - (reply: 3)
243. help us understand the run - (reply: 1)
244. Different MOI in comparison experiment - (reply: 3)
245. How to determine the size of gene to amplify? - (reply: 1)
246. Guanidine isothiocyanate in PCR - (reply: 1)
247. Untreated samples negative, how to analyze fold change? - (reply: 1)
248. Primers have worked well but now getting primer dimers? - (reply: 2)
249. I cannot design primers on exon-exon junction - (reply: 2)
250. DNA Quantification of PCR Products - (reply: 2)
251. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
252. Problem for PCR - (reply: 9)
253. Confused about my CT values - (reply: 1)
254. Designing primers in UTRs - (reply: 1)
255. Multiplex PCR - (reply: 1)
256. primer design@ buy? - (reply: 2)
257. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
258. Dissolving DNA Oligos - (reply: 2)
259. Trouble with overlap extension pcr - (reply: 3)
260. copies per ul to copies per gram tissue - (reply: 2)
261. designing primers( selecting target sequence/amplicon design) - (reply: 3)
262. Question about the RT PCR - (reply: 3)
263. PCR ready mixes with long shelf lives - (reply: 4)
264. Problem with repeatability of the standard curve - (reply: 3)
265. Influenza virus - (reply: 3)
266. Defining standards in qPCR softwares - (reply: 3)
267. How to design primer to amplify genomic DNA? - (reply: 3)
268. Overlap PCR, need help - (reply: 11)
269. Internal control for miRNA RT-PCR - (reply: 1)
270. Primers - (reply: 1)