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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
1021. Nested LA PCR - Any success? (reply: 3)
1022. Unpredictablity of PCR product - (reply: 5)
1023. total cDNA amplification by PCR - (reply: 2)
1024. Detection limit of a conventional PCR - (reply: 2)
1025. Dissolved Primer pellet in pure ethanol instead of water - (reply: 2)
1026. RNAi showing upregulation via QPCR - Help needed (reply: 3)
1027. DNA detection limit of the PCR - Calculating detection limits (reply: 4)
1028. cDNA synthesis - (reply: 3)
1029. 2 rounds PCR got problem - (reply: 2)
1030. PCR help minus strand - Primer design (reply: 1)
1031. cDNA contamination, pls help! - (reply: 1)
1032. Smear in long distance PCR - (reply: 39)
1033. TP-PCR or three primer PCR - TP-PCR or three primer PCR (reply: 9)
1034. Help - I m trying to get amplification for a new gene with new set of primers (reply: 2)
1035. can contaminating gDNA explain this? - (reply: 1)
1036. TOUCH DOWN PCR - (reply: 2)
1037. Source of RNA for pcr efficiency, when to use ref gene? - (reply: 3)
1038. Real Easy qRT-PCR tutorial Links? - Links? (reply: 2)
1039. PCR stopped working - After changing buffer (reply: 5)
1040. how to determine the amount of cDNA for qPCR - (reply: 5)
1041. Problems with SYBR Green assay - bad melting curves and bad amp efficiency (reply: 12)
1042. Standardization of HRM for methylation analysis - (reply: 4)
1043. PCR protocol questions! - (reply: 2)
1044. standard curve for qPCR - (reply: 3)
1045. TOUCH DOWN PCR NEEDS EXPLANATION - (reply: 3)
1046. About serial dilution of cDNA were amplified by real-time PCR - How to do serial dilution of cDNA (reply: 1)
1047. DNA amount calculation for PCR - (reply: 14)
1048. ChIP primer design - (reply: 1)
1049. QPCR melting curves peaks - Standard curve has one peak, samples have another (reply: 5)
1050. Using digoxigenin in PCR? - Want to create a FISH probe (reply: 2)