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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
241. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
242. Problem for PCR - (reply: 9)
243. Confused about my CT values - (reply: 1)
244. Designing primers in UTRs - (reply: 1)
245. Multiplex PCR - (reply: 1)
246. primer design@ buy? - (reply: 2)
247. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
248. Dissolving DNA Oligos - (reply: 2)
249. Trouble with overlap extension pcr - (reply: 3)
250. copies per ul to copies per gram tissue - (reply: 2)
251. designing primers( selecting target sequence/amplicon design) - (reply: 3)
252. Question about the RT PCR - (reply: 3)
253. PCR ready mixes with long shelf lives - (reply: 4)
254. Problem with repeatability of the standard curve - (reply: 3)
255. Influenza virus - (reply: 3)
256. Defining standards in qPCR softwares - (reply: 3)
257. How to design primer to amplify genomic DNA? - (reply: 3)
258. Overlap PCR, need help - (reply: 11)
259. Internal control for miRNA RT-PCR - (reply: 1)
260. Primers - (reply: 1)
261. Primers mix - (reply: 2)
262. degenerate bases in my sequences - (reply: 1)
263. Need help with dCAPS pcr, seeing huge bands on gel - (reply: 1)
264. How do I make GTE buffer for alkaline lysis? - (reply: 2)
265. Having problem with primers for qPCR - (reply: 4)
266. strange raw data - - (reply: 3)
267. need a method for oligonucleotide visualization - (reply: 5)
268. Bad fragment amplification - (reply: 4)
269. problem with ChiP q-PCR - (reply: 4)
270. suitable single-copy gene target for fungal qPCR - (reply: 4)