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文献和实验定量RT-PCR (Quantitative RT-PCR)
in the RT-PCR process include the efficiency of reverse transcription, Mg 2 / dNTPs/ primer concentrations, enzyme activity, pH, annealing temperature, cycle number, temperature variation, tube to tube variation etc. Since PCR results in a million fold
that have abolished RNase H activity in real-time RT-PCR experiments. Unlike many other qRT-PCR kits, MessageSensor includes a total RNA control, a control human GAPDH primer set, RNase inhibitor, and nucleotides, as well as a buffer additive that enables detection
as possible are advised. 50. Perform a gene-specific, nested PCR to detect the presence of a particular mRNA (now cDNA) in the samples. For optimal results, design the primers so that the primary PCR product with the outer primer pair
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