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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
301. How to prepare serial dilutions of RNA or cDNA - (reply: 3)
302. Are these primer products good enough for qPCR? - (reply: 3)
303. mtDNA to nDNA Ratio gDNA - qPCR - (reply: 1)
304. Can't get PCR with large overhang primers to work - (reply: 8)
305. Primer Efficiency across runs - (reply: 1)
306. Question about pipet tips for PCR and rtPCR - (reply: 4)
307. Taqman Probe sequence problem - (reply: 4)
308. UNG in PCR - (reply: 1)
309. Cause of random samples failing PCR? - (reply: 2)
310. Template DNA for PCR- Concrentration or Volume?? - (reply: 1)
311. RNA extraction - (reply: 3)
312. Normalization of Ct of interest to a reference Ct - (reply: 3)
313. urgent: need help with qPCR statistics - (reply: 2)
314. A question for Reverse transcription experts - (reply: 5)
315. will mRNA from different cell line lead to loss of expected product in RT PCR? - (reply: 2)
316. PCR amplification with new restriction sites troubleshooting - (reply: 2)
317. using cell line to generate standard curve - (reply: 6)
318. PCR DNA Concentration - (reply: 1)
319. 3' RACE creates too big band doesn't leave well - (reply: 1)
320. RT-PCR product- no band - (reply: 4)
321. Normalization factor - (reply: 3)
322. Understanding RACE PCR - (reply: 1)
323. SYBR Select Master Mix for CFX from Invitrogen - Storage - (reply: 4)
324. Dye for qPCR - (reply: 3)
325. Pair of primers (SYBR) with more than one amplicon product(?) - (reply: 4)
326. Wierd Bands after PCR....Confused - (reply: 9)
327. PCR with Plasmid recovered from filter paper - (reply: 6)
328. PCR amplified product size - (reply: 5)
329. Opinion: What fold change is actually considered meaningful - (reply: 2)
330. Buffers RNase decontamination - (reply: 1)