HotBegan™ Hot Start Red DNA Polymerase MasterMix

HotBegan™ Hot Start Red DNA Polymerase MasterMix

Catalog Number:
PER1486804CAN
Mfr. No.:
P0320
Price:
$307
  • Size:
    5 x 1.25 mL (250 rxn)
    Quantity:
    Add to Cart:
      • Overview
        • For a Specific, Highly Efficient & Reliable Amplifications of DNA up 160 fg, with visual Tracking of DNA Migration

          HotBegan™ Hot Start Red DNA Polymease 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.

          Advantages & Features
          ▪ Accurate & Fast visual Tracking of DNA Migration: thanks to its composition that includes Red Dye Buffer.
          ▪ High specificity: minimizes unspecific amplification.
          ▪ Efficient: prevents or minimizes primer-dimer and nonspecific products.
          ▪ Great sensitivity: amplifies from femptograms of DNA targets.
          ▪ Inactive: at Room Temperature.
          ▪ Optimized
          ▪ Powerful: amplification of targets up to 5 kb.
          ▪ Convenient: available in kits and MasterMix solution.

          Specifications
          ▪ 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.

          Includes for 250 rxn:
          – 5 x 1.25 mL HotBegan™ Hot Start Red DNA Polymerase MasterMix (2x)*
          – 1.5 mL MgCl2 Solution (50mM)**
          * Includes HotBegan™ Hot Start Taq DNA Polymerase, Red Dye buffer (2x), 0.4 mM of each dNTP, 5 mM Mg2+ and 5% Glycerol.
          **Separate tube 50 mM MgCl2 solution is provided for further optimisation. In some cases, we recommend to optimize Mg2 + concentration.

          Quality Control
          ▪ Functionally tested in PCR.
          ▪ Exempt of nucleases (endo-, exo and ribonucleases) activities guaranteed by appropriate quality tests.

          Please contact us at for specific academic pricing.

      • Properties
        • Storage
          Gel pack
          Shipping
          -20 °C

          * This product is developed, designed and sold exclusively for Research purposes and in vitro use only (RUO).

      • Applications
        • 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
        • León, Maela, et al. “Identification and Characterization of Diaporthe spp. Associated with Twig Cankers and Shoot Blight of Almonds in Spain.“ Agronomy 10.8 (2020): 1062.

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