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