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