HotBegan™ Hot Start Red-Taq MasterMix

HotBegan™ Hot Start Red-Taq MasterMix

Catalog Number:
PER1268500CAN
Mfr. No.:
P0320; P0321
Price:
$280
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      • Overview
        • HotBegan™ Hot Start Red-Taq Master Mix (2x) is an optimized ready-to-use solution containing HotBegan™ Hot Start Taq DNA Polymerase, dNTPs, MgCl2 and Stabilizers. It is inactive at room temperature and only requires addition of template, primers, and water. HotBegan™ Hot Start Taq DNA Polymerase is a Taq DNA Polymerase bound to a proprietary antibody that blocks Polymerase activity until denaturation step occurs. The heat labile antibodies are rapidly inactivated by raising the temperature (4 minutes at 95-97 °C). This prevents or minimizes primer-dimer and nonspecific products. MasterMix also contains an Agarose Loading Buffer including a Red Dye for visual tracking of DNA migration and a dense compound to facilitate the drop-down of the samples into the well Agarose Gels. Like the Taq polymerase, the enzyme has 5’→3’ polymerase activity and a weak 5’→3’ exonuclease activity but no 3’→5’ exonuclease activity (proofreading). Before enzyme activation none of enzyme activities are detectable.

          Includes for 500 rxn:
          – 10 x 1. 25 mL HotBegan™ HS Red-Taq MasterMix (2x)*
          – 1. 5 mL MgCl2 Solution (50mM)**

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          Hot Start PCR
          Other Properties
          Assay Conditions: 25mM Tris-HCl pH9.0 at 25°C, 50mM KCl, 2mM MgCl2, 0.1mg/mL gelatine, 200 µM of dATP, dGTP, dTTP, 100µM[α32-P]dCTP (0.05µCi/nmol) and 12.5 µg activated salmon sperm DNA.
          Unit Definition: One unit is defined as the amount of enzyme required to catalyse the incorporation of 10 nanomoles of dNTPs into acid-insoluble material in 30 minutes at 74 °C.
          Storage
          -20 °C.

          * This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO). The product was not tested for use in diagnostics or for drug development, nor is it suitable for administration to humans or animals.

      • Applications
        • Application
          Real-Time PCR (qPCR)
          Application Description
          PCR fragments amplification for TA or GC Cloning.
          Design for High Throughput Applications.
          Amplification from a limited DNA template or low copy number genes.
      • Reference

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