|Cat. No. MB303-0050||Size: 50 Reactions|
|Cat. No. SM303-0050||Size: 50 Reactions|
The GScript RTase is recombinant M-MLV RTase expressed in E. coli and purified to homogeneity. It has lower RNase H activity and high thermal stability. The enzyme is widely used to synthesize first-strand cDNA at temperatures up to 55°C with increased specificity, higher yields of cDNA, and more full-length product than other reverse transcriptases. It can generate cDNA from 100 bp to 12 Kb.
|First-Strand cDNA Synthesis|
1. In a sterile microfuge tube, first add:
RNA solution (10 pg~5 μg total RNA or 10 pg~500 ng mRNA)
1 μl oligo(dT)20 (50 μM), or other primers
1 μl 10 mM dNTP Mix
nuclease-free H2O to final volume of 13 μl
|2. Heat for 3-5 minutes at 65°C. Spin briefly and place promptly on ice.|
4 μl 5X RT Buffer
1 μl 0.1 M DTT
1 μl RNase Inhibitor (10 U/μl)
1 μl GScript RTase (200 units/μl)
final volume 20 μl
If generating cDNA longer than 5 kb at temperatures above 50°C using a gene-specific primer or oligo(dT)20, the amount of GScript RTase may be raised to 400 U (2 μl) to increase yield.
|4. Incubate at 50°C for 30-60 minutes. Increase the reaction temperature to 55°C for gene-specific primer.|
Reaction temperature may also be increased to 55°C for difficult templates or templates with high secondary.
|5. Inactivate enzyme at 70°C for 15 minutes.|
|6. Store products at -20°C or proceed to PCR using 2 μl first-strand cDNA synthesis reaction mixture. Amplification of some PCR targets (> 1 kb) may require the removal of RNA complememtary to the cDNA. To remove RNA complementary to the cDNA, add 1 μl (2 units) of E. coli RNase H and incubate at 37°C for 20 minutes.|
Store all components at -20°C (non-frost-free).
Thaw 5X RT Buffer, 0.1 M DTT at room temperature justprior to use and refreeze immediately.