Product Details
The kit provides all the necessary components (TransScript® II RT, RNase Inhibitor, Anchored Oligo(dT)20 Primer, Random Primer(N9), dNTPs, Buffer) for reverse transcription reaction. It is provided at 5× concentration and used by adding gDNA remover, RNA template and H2O for efficient first-strand cDNA synthesis at 42℃-55℃. Simultaneously, residual genomic DNA from RNA template can be removed. 5 ×TransScript® II All-in-One No-RT Control SuperMix for qPCR is supplied to prepare no-reverse transcriptase(RT) control, which is used to assess if the template for the qPCR reaction is contaminated with genomic DNA. This product is capable of minimizing contamination during operation with a simple workflow.
The resulting cDNA is suitable for qPCR, not for regular PCR.
• High copy and low copy gene detection
at -18℃ or below for two years
Dry ice (-70 ℃)
| Component | AH341-01 (50 rxns ) |
| 5×TransScript® II All-in-One SuperMix for qPCR | 200 μl |
| 5×TransScript® II All-in-One No-RT Control SuperMix for qPCR | 20 μl |
| gDNA Remover | 50 μl |
| RNase-free Water | 1 ml |
1 Rui C, Zhang Y, Fan Y, et al. Insight Between the Epigenetics and Transcription Responding of Cotton Hypocotyl Cellular Elongation Under Salt-Alkaline Stress[J]. Frontiers in Plant Science, 2021.(IF 5.73)
