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