Products

This product is an improved version of DpnI restriction enzyme, exhibiting higher activity compared with conventional DpnI enzyme. This enzyme can effectively recognize and cleave the sequence GmATC (A is methylated) and cannot cleave the sequence GATC (A is not methylated). DMT Enzyme is compatible with reaction buffers of multiple PCR enzymes (such as EasyPfu, TransStart, FastPfu, etc.). After PCR, this enzyme can be added directly to the reaction system to start digestion reaction. After digestion reaction, downstream transformation experiments can be performed without heat inactivation.

Restriction Site

Highlights

High efficiency, high specificity, no star activity.
 

Applications
In vitro site-directed DNA mutagenesis; degradation of methylated plasmid template
 

Storage
at -20°C  for two years
 

Shipping
Dry ice (-70 ?)