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