Bst 3.0 is derived from Bacillus stearothermophilus DNA Polymerase. Through genetic engineering technology, it retains 5'→3' DNA polymerase activity and removes 5'→3' exonuclease activity. It has strand displacement ability and can be used for DNA strand displacement reaction and LAMP (Loop-mediated isothermal amplification) amplification. Bst 3.0 DNA polymerase has been genetically modified to have higher sensitivity. Compared with wild-type Bst DNA polymerase and Bst large fragment, this enzyme can effectively improve the anti-interference performance of inhibitors, amplification speed, yield, etc. Bst 3.0 DNA polymerase can use dUTP to build LAMP anti-contamination system.
Compositions:
1. 8 U/µL Bst 3.0
2. 10×LAMP Basic Buffer (Mg²+ free)(Optional)
3. 250 mM MgSO₄(Optional)
*10×LAMP Basic Buffer (Mg²+ free) does not include dNTP or Mg²+,Please add dNTPs and MgSO₄ when preparing reaction system.
Features:
1. Suitable for LAMP amplification.
2. Strong anti-inhibition ability, high impurity tolerance with high sample compatibility.
Recommended Applications:
1. LAMP Isothermol amplification.
2. Establishment of anti-contamination system.
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