Pfu DNA Polymerase
$0.00 – $459.00
Pfu DNA Polymerase is a highly thermostable DNA polymerase from hyperthermophilic archaeum Pyrococcus furiosus.
SKU | Volumes | Concentration | Price | Quantity | ||
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AD-200 | 500 Units | 2.5 U/ul | $210.00 | |||
AD-205 | 1,000 Units | 2.5 U/ul | $334.00 | |||
AD-210 | 2,500 Units | 2.5 U/ul | $459.00 | |||
AD-OEM | Any Size | Please inquire |
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Description
Description:
Pfu DNA Polymerase is a highly thermostable DNA polymerase from hyperthermophilic archaeum Pyrococcus furiosus. The enzyme catalyzes the template-dependent polymerization of nucleotides into duplex DNA in 5′->3′ direction. Pfu DNA Polymerase also exhibits 3′->5′ exonuclease (proofreading) activity, that enables the polymerase to correct nucleotide incorporation errors. It has no 5′->3′ exonuclease activity. The main difference between Pfu and alternative enzymes is that Pfu has superior thermostability and proof-reading properties. Unlike Taq DNA polymerase, Pfu DNA polymerase also possesses 3′->5′ exonuclease proofreading activity, resulting in PCR fragments with fewer errors than Taq-generated PCR inserts. Pfu DNA polymerase is efficient for techniques that require high-fidelity DNA synthesis, but can also be used in conjunction with Taq polymerase to obtain the fidelity of Pfu with the speed of Taq polymerase activity.
Applications:
- High-fidelity PCR and primer-extension reactions
- Generation of PCR products for cloning and expression
- PCR cloning and blunt-end amplification product generation
- RT-PCR for cDNA cloning and expression
- Site-directed mutagenesis
- Blunt-end PCR cloning
Source:
Thermostable DNA polymerase from hyperthermophilic archaeon pyrococcus furiosus
Unit Definition:
One unit is defined as the amount of enzyme required to catalyze the incorporation of 10 nmol of dNTPs into acid insoluble material in 30 minutes at 74°C under standard DNA polymerase assay conditions.
Supplied With:
10x Pfu Reaction Buffer (with dNTPs)
10x Pfu Reaction Buffer (with dNTPs)
200mM Tn3 pH 8.8
20 mM MgSO4
100 mM KCl
100 mM (NH4)2SO4
1% Triton
1 mg/ml BSA
2 mM dNTP
Supplied In:
20 mM Tris-HCl (pH 8.0)
40 mM NaCl
0.1 mM EDTA
1 mM DTT
50% (v/v) glycerol
Heat Inactivation:
95% inactive after 1-hour incubation at 98°C
Recommended Reaction Conditions:
1X Pfu buffer, 200 µM each dNTP, 0.1-0.5µM each primer, 5 units Pfu DNA polymerase enzyme, 1-100ng plasmid template DNA, or 100-250ng genomic template DNA.
Recommended Storage Condition: -20ºC
Additional information
OPTIONS | 500 Units (2.5 U/ul), 1,000 Units (2.5 U/ul), 2,500 Units (2.5 U/ul), Any Size |
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Manual & Protocols
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