- Overview
- Protocols
- Specifications
- Resources
Cut Site:
CG AT?CG
GC?TA GCUsage Notes:
- Religation of DNA fragments with dam methylation is difficult.
- Ends generated by PvuI can be directly ligated to ends generated by SgfI. The PvuI site is regenerated in the ligation product, but the SgfI site is not.
Incubation Conditions: Buffer D. 37°C.
Source: Proteus vulgaris.
Storage Buffer: 10mM Tris-HCl (pH 7.3 @ 25°C), 50mM NaCl, 0.1% Triton® X-100, 1mM DTT, 0.1mM EDTA, 0.5mg/ml BSA and 50% glycerol.
Percent Activity in 4-CORE® Buffer:
A B C D MULTI-CORE™ 10–25% 25–50% 50–75% 100% <10% Frequency of Cutting:
? Ad-2 ?X174 pUC18 M13mp18 pBR322 3 7 0 2 1 1 -
Protocols
Complete Protocol
Restriction Enzyme Protocol
PDF (410 KB)
-
Certificate of Analysis
Lookup Certificate of AnalysisStorage Conditions
-30C TO -10C
Use Restrictions
For Research Use Only. Not for Use in Diagnostic Procedures.
-
Resources
Other