| Catalog | Description | Size | Price (USD) | Qty |
|---|---|---|---|---|
| 786-850 | Taq PLUS DNA Polymerase | 1000U | $115.00 |
Taq Plus DNA Polymerase is a mixture of Taq DNA Polymerase and Pfu, a proofreading DNA Polymerase, which allows for the amplification of long templates, up to 20kb, with high fidelity. The two enzymes act synergistically during PCR to generate more accurate and longer PCR products with greater yields compared to Taq DNA Polymerase alone. PCR products, amplified up to 20kb in length with Taq Plus DNA Polymerase, contain a mixture of blunt ends and single base (A) 3’ overhang. The error rate of this PCR amplification is 7.5x10-5 per nucleotide per cycle.
STORAGE BUFFER
20mM Tris.HCl (pH8.0), 100mM KCl, 3mM MgCl2, 1mM DTT, 0.1% Nonidet® P-40, 0.1% Tween® 20, 0.2mg/ml BSA, 50% (v/v) glycerol.
10X PCR BUFFER
100mM Tris-HCl (pH8.8), 500mM potassium chloride, 1% Triton® X-100, 16mM MgCl2.
UNIT DEFINITION
One unit (U) is defined as the amount of enzyme needed to catalyze the incorporation of 10 nanomoles of deoxyribonucleotides into acid-insoluble material in 30 minutes at 70°C using herring sperm DNA as a substrate.
Features
Taq Plus DNA Polymerase is a mixture of Taq DNA Polymerase and Pfu, a proofreading DNA Polymerase, which allows for the amplification of long templates, up to 20kb, with high fidelity. The two enzymes act synergistically during PCR to generate more accurate and longer PCR products with greater yields compared to Taq DNA Polymerase alone. PCR products, amplified up to 20kb in length with Taq Plus DNA Polymerase, contain a mixture of blunt ends and single base (A) 3’ overhang. The error rate of this PCR amplification is 7.5x10-5 per nucleotide per cycle.
STORAGE BUFFER
20mM Tris.HCl (pH8.0), 100mM KCl, 3mM MgCl2, 1mM DTT, 0.1% Nonidet® P-40, 0.1% Tween® 20, 0.2mg/ml BSA, 50% (v/v) glycerol.
10X PCR BUFFER
100mM Tris-HCl (pH8.8), 500mM potassium chloride, 1% Triton® X-100, 16mM MgCl2.
UNIT DEFINITION
One unit (U) is defined as the amount of enzyme needed to catalyze the incorporation of 10 nanomoles of deoxyribonucleotides into acid-insoluble material in 30 minutes at 70°C using herring sperm DNA as a substrate.
Features
