VWR®, TEMPase Hot Start DNA polymerase

VWR® TEMPase Hot Start DNA Polymerases are highly stable polymerases, featuring higher specificity, superior sensitivity and greater yields compared to standard DNA polymerases. These features make them well suited for the detection of low abundance targets. Other uses include screening, amplification of GC-rich sequences, multiplex PCR, direct PCR and qPCR. A glycerol-free TEMPase Hot Start DNA Polymerase is also available for automation and freeze drying.

The GC-Rich Template kit is specifically designed for difficult GC-rich sequences. Combined with TEMPase, GC buffers I and II promote excellent amplification. The kit is designed for initial testing before using one of the GC-TEMPase 2X Master Mixes.

: VWR® TEMPase DNA polymerases generally include two different buffers, Key Buffer and Combination Buffer, which are each suited to different PCR requirements. Key Buffer (NH⁴⁺) gives a superior amplification signal (high yield), and minimises the need for optimisation of the Mg²⁺ concentration or the annealing temperature in most primer-template systems. Combination Buffer is a mixture of K⁺ and NH⁴⁺. It combines high specificity with good product yield and high tolerance to optimisation of primer annealing temperatures and Mg²⁺ concentrations, due to its balanced ammonium-potassium formulation. Each buffer contains 15 mM MgCl₂ (1,5 mM in final volume). Additional MgCl₂ for easy optimisation is included in a separate vial.

Application:
Multiplex
Format:
Enzyme with/without buffer
High fidelity:
No
Hot start:
Chemically modified
Storage conditions:
– 20 °C (long term), + 4 °C (6 months)
Amplicon size:
≤ 5kb
Processivity:
Standard
Exonuclease activity:
5’→3’
Product overhang:
3'A
Buffer composition:
10x Key Buffer, 10x Combination Buffer and 25 mM MgCl2
Concentration:
5 U/µl
Description:
TEMPase HotStart DNA Polymerase 5U/µl 500 units
Size:
1 x 0.1 ml + 3 x 1.5 ml
Units:
500
Features:
Glycerol free

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VWR® for PCR

VWR® PCR Enzymes