Cold sensitive mutant hotstar Taq DNA Polymerase
2021-12-22
Super High Fidelity DNA Polymerase
2021-12-23
Product Number: TR02
Shipping and Storage
-20℃
Components
| Components | TR02 | TR02 |
| Thermostable T7 RNA Polymerase (50U/μl) | 100μl | 500μl |
| 10×Transcription Buffer | 1ml | 1ml×5 |
Description
Thermalstable T7 RNA Polymerase is a genetically modified T7 RNA polymerase.This enzyme highly specifically recognizes the T7 promoter sequence and can perform efficient in vitro transcription at 50℃.During the in vitro transcription process, it can improve the capping efficiency and eliminate the production of dsRNA byproducts.
Features
The T7 promoter has high specificity and is used for the synthesis of in vitro RNA (including small RNAs).
Application
- Synthesis of single stranded RNA;
- Synthesis of highly specific RNA probes;
- Synthesis of siRNA precursors;
- Produce precursors for RNA splicing reactions;
- Using cap analog as a primer, produce Capped mRNA.
Unit definition
The amount of enzyme required to mix 1 nmol of [3H] GMP with acid insoluble precipitate within 1 hour at 50℃ and pH 8.0 is defined as 1 active unit.
Quality Control
After multiple column purification, SDS-PAGE gel detection only showed clear and single target bands, with a purity of 95%. PCR detection showed no residual Escherichia coli DNA and no contamination of RNase, nucleic acid endonucleases, and exonucleases.
Suggestions
- For effective transcription in specific regions, it is recommended to pre cut the template DNA into flat or 5 'protruding ends downstream of the region.
- The binding of spermidine in the buffer with nucleic acid may form insoluble substances, and it is recommended to add template DNA finally.
Order
| TR02 | Thermostable T7 RNA Polymerase | 50U/μl |
