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271. Guanidine isothiocyanate in PCR - (reply: 1)
272. Untreated samples negative, how to analyze fold change? - (reply: 1)
273. Primers have worked well but now getting primer dimers? - (reply: 2)
274. I cannot design primers on exon-exon junction - (reply: 2)
275. DNA Quantification of PCR Products - (reply: 2)
276. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
277. Problem for PCR - (reply: 9)
278. Confused about my CT values - (reply: 1)
279. Designing primers in UTRs - (reply: 1)
280. Multiplex PCR - (reply: 1)
281. primer design@ buy? - (reply: 2)
282. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
283. Dissolving DNA Oligos - (reply: 2)
284. Trouble with overlap extension pcr - (reply: 3)
285. copies per ul to copies per gram tissue - (reply: 2)
286. designing primers( selecting target sequence/amplicon design) - (reply: 3)
287. Question about the RT PCR - (reply: 3)
288. PCR ready mixes with long shelf lives - (reply: 4)
289. Problem with repeatability of the standard curve - (reply: 3)
290. Influenza virus - (reply: 3)
291. Defining standards in qPCR softwares - (reply: 3)
292. How to design primer to amplify genomic DNA? - (reply: 3)
293. Overlap PCR, need help - (reply: 11)
294. Internal control for miRNA RT-PCR - (reply: 1)
295. Primers - (reply: 1)
296. Primers mix - (reply: 2)
297. degenerate bases in my sequences - (reply: 1)
298. Need help with dCAPS pcr, seeing huge bands on gel - (reply: 1)
299. How do I make GTE buffer for alkaline lysis? - (reply: 2)
300. Having problem with primers for qPCR - (reply: 4)
272. Untreated samples negative, how to analyze fold change? - (reply: 1)
273. Primers have worked well but now getting primer dimers? - (reply: 2)
274. I cannot design primers on exon-exon junction - (reply: 2)
275. DNA Quantification of PCR Products - (reply: 2)
276. In 2^ minus ddCt method, why is the "minus" sign? - (reply: 1)
277. Problem for PCR - (reply: 9)
278. Confused about my CT values - (reply: 1)
279. Designing primers in UTRs - (reply: 1)
280. Multiplex PCR - (reply: 1)
281. primer design@ buy? - (reply: 2)
282. High Ct/Cq values in my NO-RT and NTC samples - (reply: 3)
283. Dissolving DNA Oligos - (reply: 2)
284. Trouble with overlap extension pcr - (reply: 3)
285. copies per ul to copies per gram tissue - (reply: 2)
286. designing primers( selecting target sequence/amplicon design) - (reply: 3)
287. Question about the RT PCR - (reply: 3)
288. PCR ready mixes with long shelf lives - (reply: 4)
289. Problem with repeatability of the standard curve - (reply: 3)
290. Influenza virus - (reply: 3)
291. Defining standards in qPCR softwares - (reply: 3)
292. How to design primer to amplify genomic DNA? - (reply: 3)
293. Overlap PCR, need help - (reply: 11)
294. Internal control for miRNA RT-PCR - (reply: 1)
295. Primers - (reply: 1)
296. Primers mix - (reply: 2)
297. degenerate bases in my sequences - (reply: 1)
298. Need help with dCAPS pcr, seeing huge bands on gel - (reply: 1)
299. How do I make GTE buffer for alkaline lysis? - (reply: 2)
300. Having problem with primers for qPCR - (reply: 4)