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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
901. 2 rounds PCR got problem - (reply: 2)
902. PCR help minus strand - Primer design (reply: 1)
903. cDNA contamination, pls help! - (reply: 1)
904. Smear in long distance PCR - (reply: 39)
905. TP-PCR or three primer PCR - TP-PCR or three primer PCR (reply: 9)
906. Help - I m trying to get amplification for a new gene with new set of primers (reply: 2)
907. can contaminating gDNA explain this? - (reply: 1)
908. TOUCH DOWN PCR - (reply: 2)
909. Source of RNA for pcr efficiency, when to use ref gene? - (reply: 3)
910. Real Easy qRT-PCR tutorial Links? - Links? (reply: 2)
911. PCR stopped working - After changing buffer (reply: 5)
912. how to determine the amount of cDNA for qPCR - (reply: 5)
913. Problems with SYBR Green assay - bad melting curves and bad amp efficiency (reply: 12)
914. Standardization of HRM for methylation analysis - (reply: 4)
915. PCR protocol questions! - (reply: 2)
916. standard curve for qPCR - (reply: 3)
917. TOUCH DOWN PCR NEEDS EXPLANATION - (reply: 3)
918. About serial dilution of cDNA were amplified by real-time PCR - How to do serial dilution of cDNA (reply: 1)
919. DNA amount calculation for PCR - (reply: 14)
920. ChIP primer design - (reply: 1)
921. QPCR melting curves peaks - Standard curve has one peak, samples have another (reply: 5)
922. Using digoxigenin in PCR? - Want to create a FISH probe (reply: 2)
923. weird QPCR curves - (reply: 2)
924. how many minimum and maximum number of bands in SSCP marker? - (reply: 2)
925. Questions regarding RT-PCR optimization - (reply: 2)
926. Problems with semi-quatitative PCR - (reply: 1)
927. conversion of total RNA to cDNA - problems in total RNA to cDNA (reply: 7)
928. Long-amplicon QPCR of mtDNA - (reply: 5)
929. PCR reaction calculation - (reply: 2)
930. Qiagen rotorgene syber green kit reaction volume - (reply: 1)