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