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Top : New Forum Archives (2009-): : PCR--RT-PCR-and-Real-Time-PCR
961. semiquantitative pcr - (reply: 1)
962. difference in band sizes ! - why ??? (reply: 2)
963. PCR product - (reply: 5)
964. choosing new taq - (reply: 8)
965. pcr amplify an insert in plasmid? - (reply: 2)
966. Sybr Green Real Time PCR - Amplification plot - Any problem? (reply: 1)
967. Exon Spanning PCR Primers - (reply: 1)
968. Primer sequences - (reply: 1)
969. Nuclear or Cytoplasmic RNA Purification - (reply: 1)
970. >100% qPCR efficiency - (reply: 2)
971. Why does freezing/thawing DNA samples first improve PCR results? - (reply: 8)
972. PCR Primers - (reply: 2)
973. Cleaning up RT-PCR product before sequencing - (reply: 1)
974. reference gene - (reply: 2)
975. Improving qRT-PCR detection limits - (reply: 2)
976. What to use for Standard Curve - (reply: 2)
977. gPCR - (reply: 1)
978. RT-PCR cDNA synthesis - (reply: 6)
979. problems amplifying from cDNA - (reply: 4)
980. Real-time PCR about Incorrect setup of the data collection stage - (reply: 1)
981. Primers... - (reply: 1)
982. 18s as endogenous control for Oligo dT RT - Can we use 18s ? (reply: 2)
983. excel and propagation of error, qpcr - (reply: 1)
984. Reverse transcription (cDNA synthesis) curiosity and confusion - Does the amount of RNA have to be doubled if you double everything els (reply: 4)
985. primer with higher melting temperature - (reply: 2)
986. Omitting Points in Standard Curve - (reply: 2)
987. Triage of miRNA targets by qPCR - (reply: 1)
988. Smallest reaction volume with Roche Lightcycler 480 96-well plate format - (reply: 2)
989. qPCR primer design - possible off-target (reply: 1)
990. Primer dimer formation and real-time PCR - (reply: 7)