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