Bst 2.0

Bst DNA Polymerase is derived from Bacillus stearothermophilus DNA PolymeraseⅠ. Through genetic engineering technology, the 5'→3' DNA polymerase activity is retained, while the 5'→3' exonucepase activity is removed, and it has strand displacement ability. It can be used for DNA strand displacement reactions and LAMP (Loop-mediated isothermal amplification) amplification, etc. Bst 2.0 DNA polymerase has been genetically modified to have higher sensitivity. Compared with wild-type Bst DNA polymerase and large Bst fragments, this enzyme can effectively increase amplification speed, yield, etc.

1．8 U/µL Bst 2.0 

2．10×LAMP Basic Buffer (Mg²+ free)（选配） 

3.250 mM MgSO₄ (optional)

*10×LAMP Basic Buffer (Mg²+ free) does not contain dNTP and Mg²+. Please add dNTPs and MgSO₄ when preparing the reaction system.

1. For LAMP

2. Genetically modified, it has a higher sensitivity.

Compared with wild-type Bst DNA polymerase and large fragments, Bst 2.0 effectively increases the amplification speed and yield.

lamp isothermal amplification related technologies