HS Prime Taq DNA Polymerase is designed for hot-start PCR, a technique that enhances the specificity, sensitivity and yield of DNA amplification. In addition, the enzyme provides the convenience of reaction set-up at room temperature. The enzyme is inactived at room temperature, avoiding extension of non-specifically annealed primers or primer dimers and providing higher specificity of DNA amplification. The functional activity of the enzyme is restored during 10 minute incubation at 94℃. The activated enzyme maintains the same functionality as Taq DNA Polymerase.: it catalyzes 5’→3’ synthesis of DNA, has no detectable 3‘→5’ proofreading exonuclease activity.

HS Prime Taq Premix contains HS Prime Taq DNA Polymerase, reaction buffer, dNTPs mixture, enzyme stabilizer, loading dye, and optimizes the convenience to use by adding sediment for electrophoresis.

HS Prime Taq DNA Polymerase is designed for hot-start PCR, a technique that enhances the specificity, sensitivity and yield of DNA amplification. In addition, the enzyme provides the convenience of reaction set-up at room temperature. The enzyme is inactived at room temperature, avoiding extension of non specifically annealed primers or primer dimers and providing higher specificity of DNA amplification. The functional activity of the enzyme is restored during 10 minute incubation at 94℃. The activated enzyme maintains the same functionality as Taq DNA polymerase: it catalyzes 5’→3’ synthesis of DNA, has no detectable 3‘→5’ proofreading exonuclease activity.