HyperScript™ RT SuperMix for qPCR
HyperScript™ RT SuperMix for qPCR is the premixed solution for reverse transcription reaction, based on HyperScript™ Reverse Transcriptase (Cat. No. K1071). HyperScript™ Reverse Transcriptase is a new enzyme obtained through genetic engineering based on M-MLV (RNase H-) Reverse Transcriptase. In comparison, HyperScript™ Reverse Transcriptase reduces RNase H activity and increases thermal stability. HyperScript™ Reverse Transcriptase can withstand higher reaction temperatures and is suitable for reverse transcription of RNA templates with complex secondary structures.
HyperScript™ RT SuperMix for qPCR is suitable for two-step qRT-PCR detection ,5X RT SuperMix contains all the components required for reverse transcription, and the reaction can be carried out quickly by only adding template RNA and RNase Free ddH2O. the volume of the RNA template can be added up to 80% of the total volume, which is very suitable for the reverse transcription reaction of the low concentration RNA template. 5X RT SuperMix will not freeze at -20°C, easy to use. This product is specially optimized for qPCR. the proportionally optimized Oligo (dt)23vn primer mix/random primers enables cDNA synthesis to start from various regions of the RNA transcript with the same reverse transcription efficiency, maximizing the authenticity and repeatability of the qPCR results. The reverse transcription products are suitable for qPCR by Green and probe methods. The corresponding reagents can be selected for high performance gene expression analysis according to the experimental purpose.
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| Components | 50 rxns (20 μL reaction) | 100 rxns (20 μL reaction) |
| RNase Free ddH2O | 1 mL | 1 mL x 2 |
| 5X RT SuperMix | 200 μL | 400 μL |
| 5X No RT control Mix | 20 μL | 40 μL |
Store the components at -20°C. | ||
5X RT SuperMix contains all the ingredients required for reverse transcription and is easy to operate;
The optimized ratio of Oligo (dT)23VN primers to random primers can ensure the authenticity and repeatability of qPCR results to the greatest extent;
Efficient Reverse Transcriptase for RNA templates containing secondary structures;
Detects template starting amounts as low as 1 pg;
Oligo (dT)23VN primers have stronger template anchoring ability and higher reverse transcription efficiency than Oligo (dT)18.