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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
241. Taqman Probe sequence problem - (reply: 4)
242. UNG in PCR - (reply: 1)
243. Cause of random samples failing PCR? - (reply: 2)
244. Template DNA for PCR- Concrentration or Volume?? - (reply: 1)
245. RNA extraction - (reply: 3)
246. Normalization of Ct of interest to a reference Ct - (reply: 3)
247. urgent: need help with qPCR statistics - (reply: 2)
248. A question for Reverse transcription experts - (reply: 5)
249. will mRNA from different cell line lead to loss of expected product in RT PCR? - (reply: 2)
250. PCR amplification with new restriction sites troubleshooting - (reply: 2)
251. using cell line to generate standard curve - (reply: 6)
252. PCR DNA Concentration - (reply: 1)
253. 3' RACE creates too big band doesn't leave well - (reply: 1)
254. RT-PCR product- no band - (reply: 4)
255. Normalization factor - (reply: 3)
256. Understanding RACE PCR - (reply: 1)
257. SYBR Select Master Mix for CFX from Invitrogen - Storage - (reply: 4)
258. Dye for qPCR - (reply: 3)
259. Pair of primers (SYBR) with more than one amplicon product(?) - (reply: 4)
260. Wierd Bands after PCR....Confused - (reply: 9)
261. PCR with Plasmid recovered from filter paper - (reply: 6)
262. PCR amplified product size - (reply: 5)
263. Opinion: What fold change is actually considered meaningful - (reply: 2)
264. Buffers RNase decontamination - (reply: 1)
265. the storage time for primers - (reply: 9)
266. Annealing temperature for PCR - (reply: 8)
267. can canine COL1A1 primers be used to quantify human COL1A1 cDNA in qPCR - (reply: 1)
268. Nested PCR - (reply: 2)
269. random primers or oligodT - (reply: 4)
270. Confused about normalization - (reply: 2)