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Description
5'...G T^A C...3'
3'...C A^T G...5'
Supplied with: 10X OPTIZYME Buffer 4
Conditions for 100% Activity:
- 1X OPTIZYME Buffer 4: 33mM Tris-acetate (pH 7.9 at 37°C), 10mM Mg-acetate, 66mM K-acetate and 0.1mg/ml BSA
- Incubate at 37°C
- Buffer 1: 50 - 100%
- Buffer 2: 20 - 50%
- Buffer 3: 0 - 20%
- Buffer 4: 100%
- Buffer 5: 0 - 20%
- 10mM Tris-HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/ml BSA and 50% (v/v) glycerol
- More than 95% of the DNA fragments can be ligated and re-cut after a 50-fold over-digestion with RsaI
- 5'...GTAm5C G...3'
- 5'...m5C GTAm5C G...3'
Specifications
Specifications
| Concentration | 10 U/μL |
| Components | >50% Glycerin, 25 to 50% Water |
| Incubator Temperature | 37°C |
| pH | 7.4 |
| For Use With (Application) | >90% of DNA fragments can be ligated and re-cut after 10-fold over-digestion with Rsa I |
| Storage Buffer | 10mM Tris HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
| Content And Storage | Keep container tightly closed |
| Quantity | 1000 U |
| Cut Site | GT.AC |
| Product Type | RsaI |
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