Overview:

The fidelity of Taq Plus is 6 times greater than that of Taq DNA Polymerase. Taq Plus also has stronger amplification performance, higher sensitivity and yield and is more tolerant of impurities within 5 kb amplifying range, compared to Taq DNA Polymerase. The resulting PCR products contain A at the 3’-end and can be directly cloned into T-Vectors

Applications of this product include routine PCR amplification of DNA fragments, generation of PCR products for TA cloning, DNA labelling and DNA sequencing.

References:

1. Innis M A, et al: PCR protocols and applications: A laboratory manual, academic, New York, 1989.
2. Innis M A, et al: DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA, Proc. Natl. Acad. Sci. USA. 1988, 85:9436-9440.
3. Weyant R S, et al: Effect of ionic and nonionic detergents on the Taq polymerase. Biotechniques. 1990, 9:308-309.