
Taq 2x PCR Master Mix is a ready-to-use reaction mix for sensitive, robust and fast PCR. The combination of aptamer-based fast-start Taq DNA polymerase, optimized reaction buffer and ultrapure dNTPs ensures consistent results, rapid set-up time and lower risk of pipetting errors. The Taq DNA polymerase has a 5'-3'-exonuclease activity and therefore, can be used for hydrolysis probe-based real-time PCRs. It provides a robust PCR performance for a wide range of PCR applications in all standard PCR cyclers.
Storage | -20°C |
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Shipping | Cold packs |
References:
Lawyer, F. C., Stoffel, S., Saiki, R. K., Myambo, K., Drummond, R., & Gelfand, D. H. (1989). Isolation, characterization, and expression in Escherichia coli of the DNA polymerase gene from Thermus aquaticus. Journal of Biological Chemistry, 264(11), 6427-6437.
Tindall, K. R., & Kunkel, T. A. (1988). Fidelity of DNA synthesis by the Thermus aquaticus DNA polymerase. Biochemistry, 27(16), 6008-6013.
Saiki, R. K., Gelfand, D. H., Stoffel, S., Scharf, S. J., Higuchi, R., Horn, G. T., ... & Erlich, H. A. (1988). Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science, 239(4839), 487-491.
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