TransGen Biotech TransScript II Probe One Step qRT PCR SuperMix One step RT PCR Master Mix Nucleic Acid Test Kit RT PCR Test Kit

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Product Overview

Description


Cat. No.  AQ321


Ordering Information:














AQ321-01



100 rxns (20 μl per reaction)



AQ321-02



400 rxns (20 μl per reaction)



 


Storage:  at -20°C for two years


Shipping: Dry ice (-70 ℃)


 


Description


TransScript® II Probe One-Step qRT-PCR SuperMix is a one-step qRT-PCR kit with high sensitivity, high synthesis efficiency and high amplification efficiency. It contains all the necessary reagents for cDNA synthesis and qPCR except probe, total RNA/mRNA template and gene specific primers.


 


• High specificity, high sensitivity, high efficiency.


• Easy and rapid, reducing contamination.


• Compatibility with various real-time cyclers with passive reference dyes provided for different qPCR instruments.


  


Applications


• Multiple copy and low copy gene detection


• GC-rich templates or complex secondary structure RNA templates


• Viral RNA and trace RNA detection


 


Kit Contents































Component



AQ321-01



AQ321-02



TransScript® II One-Step RT/RI  Enzyme Mix



40 μl



160 μl



TransStart®Probe qPCR SuperMix



1 ml



4×1 ml



Passive Reference Dye (50×)



40 μl



160 μl



RNase-free Water



1 ml



4×1 ml



 


Reaction Components























































ComponentVolumeFinal Concentration
RNA Template Variable as required
Forward GSP (10 μM)  0.4 μl 0.2 μM
Reverse GSP (10 μM)  0.4 μl 0.2 μM
Probe (10 µM) 0.4 μl 0.2 µM
TransStart® Probe qPCR SuperMix 10 μl
TransScript® II One-Step RT/RI Enzyme Mix 0.4 μl -
Passive Reference Dye (50×) (optional)  0.4 μl
RNase-free Water Variable  -
Total volume  20 μl -

 


Notes


• Avoid any RNase contamination.


• High quality RNA template is recommended for use to ensure successful cDNA synthesis.


• This kit is only suitable for GSP, but unsuitable for first-strand cDNA synthesis using Oligo(dT) or Random Primer. 


 


  


 


 


 


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