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