Life Science
Code No. TRT-101 10,000U
*This product is not available in the US.
High Efficient Reverse Transcription Kit
ReverTra Ace -α-®
Description
ReverTra Ace-α-® is an efficient and convenient kit to synthesize high quality cDNA. This kit contains the highly efficient reverse transcriptase "ReverTra Ace®", as well as other components optimized for the synthesis of long cDNAs suitable for RT-PCR. ReverTra Ace® is an M-MLV reverse transcriptase that has been improved by point mutation technology. ReverTra Ace® has two mutations in the polymerase and RNase H domains.
Features
- Contains all components for reverse transcription.
- Enables the synthesis of ≥ 14 kb cDNA.
Applications
- cDNA synthesis
- RT-PCR
Storage condition
Store at -20°C
Components
ReverTra Ace® | 100 µl |
---|---|
5xRT buffer (contains 25 mM Mg2+) | 400 µl |
Rnase inhibitor (10 U/µl) | 100 µl |
dNTPs mixture (10 mM) | 200 µl |
RNase-free H2O | 1200 µl |
Oligo (dT)20 (10 pmol/µl) | 100 µl |
Random primers (25 pmol/µl) | 100 µl |
Control Primer F (10 pmol/µl) | 50 µl |
Control Primer R (10 pmol/µl) | 50 µl |
Positive control RNA (105 copies/µl) | 50 µl |
Application data
Example 1. Detection of human β-actin mRNA by RT-PCR utilizing ReverTra Ace-α-® and various PCR enzymes
cDNA was synthesized using 1 mg total RNA from the human cell line (HeLa cell) at 42ºC for 20 minutes, followed by inactivation with ReverTra Ace-α-® in a volume of 20 ml at 99ºC for 5 minutes. Subsequently, using the attained cDNA, the target gene (β-actin: 838 bp) was amplified with various PCR enzymes.As shown in Fig. 1, the target genes were successfully amplified using the various PCR enzymes tested.
M: 100 bp Ladder Marker
1: rTth DNA polymerase
2: rTaq DNA polymerase
3: High efficient Taq DNA polymerase (Company A)
4: High efficient Taq DNA polymerase (Company B)
5: KOD Dash [Code No. LDP-101]
Fig. 1 Amplification of the 838-bp β-actin gene
References
- W.M. Barns, PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.
Proc. Natl. Acad. Sci. USA, 91: 2216-2220 (1994)
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