The GoTaq® Probe qPCR Master Mix is optimized for fast reproducible quantitative PCR assays in the hydrolysis probe detection format. The master mix is provided as a ready-to-use, stabilized 2X formulation contains GoTaq® Hot Start Polymerase, MgCl2, dNTPs a proprietary reaction buffer. This master mix does not contain a reference dye; a separate tube of CXR reference dye is included. The GoTaq® Probe 2-Step RT-qPCR System facilitates detection relative quantification of RNA expression levels via a two-step RT-qPCR method using integrated components: GoScript™ Reverse Transcription System GoTaq® Probe qPCR Master Mix. The GoScript™ Reverse Transcription System includes an optimized reaction buffer M-MLV reverse transcriptase designed to enable efficient synthesis of first-strand cDNA in preparation for PCR amplification. The cDNA product can be added directly to downstream qPCR amplification reactions. The GoTaq® Probe 1-Step RT-qPCR System enables detection relative quantification of RNA expression levels using a one-step RT-qPCR method, combining GoScript™ Reverse Transcriptase GoTaq® Probe qPCR Master Mix in a single-step real-time amplification reaction. The GoScript™ RT Mix for 1-Step RT-qPCR (50X) combines optimized quantities of GoScript™ Reverse Transcriptase, RNasin® Plus RNase Inhibitor additives to enhance single-step reactions. The GoTaq® Probe qPCR Master Mix includes dUTP. When dUTP is incorporated the amplification products, the amplicons are susceptible to degradation by uracil-DNA glycosylase (UNG); allowing users to incorporate UNG subsequent reactions for control of possible carryover contamination. 特点 - 优点
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