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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1171. Help: Very odd amplification graphs (RTPCR) - (reply: 3)
1172. Help with Multiplex Nested PCR - (reply: 2)
1173. Relative quantification analysis Ct values & 2-ΔΔCT method - samples which do not amplify (reply: 5)
1174. trembling dissociation curves in HRM assays - (reply: 3)
1175. Fluorescein storage? - (reply: 2)
1176. Taq polymerase works but Phusion polymerase doesn't - How to achieve high-fidelity with robust amplification? (reply: 3)
1177. Question of q-pcr primer design - Tm difference from IDTDNA (reply: 2)
1178. TELO2 & GAPDH - (reply: 2)
1179. PCR -No band formation - (reply: 1)
1180. 3' race - (reply: 1)
1181. PCR AMPLIFICATION - (reply: 1)
1182. internal control for genomic DNA - (reply: 1)
1183. qPCR Data Analysis - Software (reply: 3)
1184. Gene expression confusion - (reply: 5)
1185. real time pcr need advise - (reply: 2)
1186. Opinion about LUX primers /D-LUX assay - What say you? (reply: 5)
1187. ChIP-qPCR shift in melt curve - (reply: 4)
1188. Long PCR Primers? Advice for generating multiple adjacent mutations - Designing long degenerate primers for shotgun alanine scanning (reply: 3)
1189. use of housekeeping gene in RT PCR chIP - (reply: 3)
1190. what is the order you follow in the run ??? - in order to make the contamination risk the least (reply: 3)
1191. DNA pooling for PCR - Saving money PCR (reply: 7)
1192. Real Time PCR Standard curves - How many are required??? (reply: 1)
1193. pcr-rflp - (reply: 2)
1194. PCR need some help - (reply: 4)
1195. problems when use qPCR to quantify bisulfite modified DNA - (reply: 4)
1196. Left polymerase out overnight - Will it still work? (reply: 1)
1197. very low expression of a sample vs standard curve efficiency - (reply: 1)
1198. Primer Reconstitution--does temperature matter? - (reply: 5)
1199. TaqMan Gene Expression Assays - Low expression/ Ct values (reply: 2)
1200. Gradient PCR works, but single temperature does not! HELP!! - (reply: 5)