Modifying Enzymes
  • GD111.JPG

DMT Enzyme (DpnI) 

Product Details

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



High efficiency, high specificity, no star activity.

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

at -20°C  for two years

Dry ice (-70 ℃)

Product Contents

DMT Enzyme200 units5×200 units
10×FlyCut® Buffer250 μl1 ml
6×DNA Loading Buffer1 ml1 ml


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