Taq Plus DNA Polymerase

Taq Plus DNA Polymerase, a mixture of Taq and Pfu polymerases, blends the processivity of Taq with the high fidelity of Pfu. Taq Plus allows amplification of the higher fidelity and longer templates than the single-enzyme formulations. It is also a better choice for amplifying complex template, such as GC-rich and secondary structure-harboring template.

More details

CAD$40.00

  • 250 U
  • 1000 U

More info

Taq Plus DNA Polymerase, a mixture of Taq and Pfu polymerases, blends the processivity of Taq with the high fidelity of Pfu. Taq Plus allows amplification of the higher fidelity and longer templates than the single-enzyme formulations. It is also a better choice for amplifying complex template, such as GC-rich and secondary structure-harboring template. And it is suitable as a direct replacement for ordinary Taq Polymerase in most applications. In addition, Using Taq plus results in 3´-dA overhangs PCR products, which can be used in TA clone.

Features
High fidelity: Its fidelity is four times higher than ordinary Taq polymerase.
High yields: Suitable for amplifying large fragment, suitable for complex template which is rich in GC or repeat sequence.

Applications
Long PCR with high fidelity
Amplification reaction of complex template

PCR of difficult targets.

Quality Control
The absence of endodeoxyribonucleases, exodeoxyribonucleases and ribonucleases confirmed by appropriate quality tests

Functionally tested in PCR

Definition of Activity Unit
One unit is defined as the amount of the enzyme required to catalyze the incorporation of 10 nM of dNTPs into an acid-insoluble form in 30 minutes at 70°C using hering sperm DNA as substrate.

Storage Buffer

20mM TrisCl ( pH8.0), 100mM KCl, 3mM MgCl2 1mM DTT,0.1% NP-40 ,0.1% Tween20, 0.2mg/ml BSA, 50% (v/v) glycerol


10X PCR Buffer

100mM Tris-HCl(PH 8.8), 500mMKCl, 1%Triton-X-100, 16mM MgCl2

Store all components at –20°C

30 other products in the same category: