Bst DNA Polymerase Large Fragment 2.0: A Next-Generation Enzyme Powering Isothermal Amplification

Bst DNA Polymerase Large Fragment 2.0, is a high-performance DNA polymerase that has been genetically engineered and optimized for process efficiency. It perfectly retains the core activity required for isothermal amplification:

1.Powerful 5'→3' DNA polymerase activity, efficiently synthesizing new chains.

2.Excellent strand displacement activity, which can unwind double-stranded DNA without a denaturation step, is the key to achieving isothermal amplification!

3.Without 5'→3' exonuclease activity, effectively preventing the degradation of amplification products and ensuring the integrity and high yield of the reaction.More importantly, Bst 2.0 has achieved a significant surpass over the wild-type Bst in multiple key performance indicators!

? Rapid amplification speed: Compared with the wild-type Bst, Bst 2.0 significantly improves the amplification speed and can complete the nucleic acid amplification cycle faster.

? Strong heat resistance：In the face of high-temperature reaction environments, Bst 2.0 can still function stably, and its enzyme activity is not affected by temperature fluctuations.

? Inhibitor-resistant: In terms of amplification speed, salt tolerance, heat resistance, and inhibitor tolerance, it outperforms the wild type and is very suitable for contamination-resistant isothermal amplification reactions.

? Batch Consistency: The production process follows the ISO 9001 quality management system to ensure consistency between production batches.

Rapid Detection of Pathogenic Microorganisms (Viruses, Bacteria, Fungi, etc.)

Point-of-Care Testing (POCT) and Bedside Diagnosis

Food Safety and Animal Disease Surveillance

Identification of Genetically Modified Components

Environmental Microbial Monitoring

Genotyping and SNP Detection

Isothermal Amplification Experiments in Basic Scientific Research