Taq plus DNA Polymerase

English name：Taq plus DNA Polymerase
Other name: Taq plus DNA polymerase

Grade：BR

Purity：≥99.0%
Concentration：5u/ul
Activity definition:The amount of enzyme required to infiltrate 10nmol isotope labeled dNTP into de81 paper insoluble matter at 72 ℃ and 30 minutes.

Product composition：Taq plus DNA Polymerase ；10×Taq Plus Buffer

10×Taq Plus Buffer：200mM Tris-HCL(PH8.8), 100mM KC1, 100mM (NH4)2SO4，20mM Mg2SO4, 1% Triton X-100, 1mg/ml BSA
Storage buffer：20mM Tris-HCL(PH8.0), 0.1mM EDTA, 1mM DTT, 0.5%(V/V) Tween 20，0.5%(v/v) Nonidet P40和50%(v/v) glycerol.

Physicochemical properties: Liquid.Taq plus DNA polymerase is a DNA polymerase prepared by special process. It is a mixed enzyme of common Taq enzyme mixed with a certain proportion of PFU enzyme. The purity of each enzyme is more than 95%. After detection, there is no nuclease and foreign DNA pollution. It has the super amplification ability of Taq enzyme. At the same time, due to the existence of PFU enzyme, it can partially correct the errors in DNA amplification, and the fidelity is about 3 times that of Taq enzyme.

Purpose: Biochemical research. After testing, there was no activity of exogenous nuclease. Taking lambda DNA as template, 2KB DNA fragment could be amplified well. It can be used for routine PCR amplification, high fidelity amplification and expression of genes, and site directed mutation of genes.