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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1261. PCR -No band formation - (reply: 1)
1262. 3' race - (reply: 1)
1263. PCR AMPLIFICATION - (reply: 1)
1264. internal control for genomic DNA - (reply: 1)
1265. qPCR Data Analysis - Software (reply: 3)
1266. Gene expression confusion - (reply: 5)
1267. real time pcr need advise - (reply: 2)
1268. Opinion about LUX primers /D-LUX assay - What say you? (reply: 5)
1269. ChIP-qPCR shift in melt curve - (reply: 4)
1270. Long PCR Primers? Advice for generating multiple adjacent mutations - Designing long degenerate primers for shotgun alanine scanning (reply: 3)
1271. use of housekeeping gene in RT PCR chIP - (reply: 3)
1272. what is the order you follow in the run ??? - in order to make the contamination risk the least (reply: 3)
1273. DNA pooling for PCR - Saving money PCR (reply: 7)
1274. Real Time PCR Standard curves - How many are required??? (reply: 1)
1275. pcr-rflp - (reply: 2)
1276. PCR need some help - (reply: 4)
1277. problems when use qPCR to quantify bisulfite modified DNA - (reply: 4)
1278. Left polymerase out overnight - Will it still work? (reply: 1)
1279. very low expression of a sample vs standard curve efficiency - (reply: 1)
1280. Primer Reconstitution--does temperature matter? - (reply: 5)
1281. TaqMan Gene Expression Assays - Low expression/ Ct values (reply: 2)
1282. Gradient PCR works, but single temperature does not! HELP!! - (reply: 5)
1283. Oligonucleotide degradation - (reply: 1)
1284. Primer efficiency - How to determine primer efficiency correctly? (reply: 4)
1285. never get bands by pfu related enzymes - (reply: 2)
1286. Primer design for qPCR - (reply: 1)
1287. Primer-BLAST... - (reply: 4)
1288. reporting results of qPCR - (reply: 1)
1289. a question about 16s rRNA as reference in RT-qPCR - (reply: 1)
1290. PCR genomic DNA of high GC content - (reply: 6)