VWR® Taq DNA Polymerase is an ultra-pure, thermostable, recombinant DNA polymerase, which provides robust PCR performance in a wide range of PCR applications, without time-consuming optimisation. The enzyme is isolated from Thermus aquaticus, and has a molecular weight of approximately 94 kDa. VWR® Taq DNA Polymerase has both a 5' to 3' DNA polymerase and a double strand 5' to 3' exonuclease activity. It leaves an A overhang, which makes the enzyme ideal for TA cloning.
- Ideal choice for routine applications
- High performance, thermostable DNA polymerase
- Optimal for TA cloning
Taq DNA polymerase concentration: 5 Units/μl
10X Key Buffer: Tris-HCl pH 8,5; (NH₄)₂SO₂, 15 mM MgCl₂, 1% Tween® 20
10X Extra Buffer: Tris-HCl pH 8,3; KCl, 15 mM MgCl₂, 1% Triton™ X-100
10X Mg-Free Key Buffer: Tris-HCl pH 8,5; (NH₄)₂SO₂, 1% Tween® 20
10X Mg-Free Extra Buffer: Tris-HCl pH 8,3; KCl, 1% Triton™ X-100
EU = Units
- Application:
- Environmentally Preferable:
TDS Taq DNA Polymerase, VWR TDS VWR Taq DNA Polymerase 1000 Units TDS VWR Taq DNA Polymerase 1000 Units with 10x Extra Buffer (Mg2+ free and Triton free) TDS VWR Taq DNA Polymerase 1000 Units with 10x Key Buffer (15 mM MgCl2) with 10x Extra Buffer (15 mM MgCl2) TDS VWR Taq DNA Polymerase 1000 Units with 10x Key Buffer (15 mM MgCl2, Tween free)