Thermo Scientific™ DreamTaq DNA Polymerase

Get higher sensitivity, longer PCR products and higher yields in all standard PCR applications with this enhanced Taq DNA polymerase.

Overview
Brand: Thermo Scientific™

Manufacturer Part Number: EP0704

DREAMTAQ DNA POL 5U/UL 20X500U

UNSPSC: 12352204

Code: 88

Additional Details:
Additional Details: Weight: 0.23000kg



Disclaimers: In certain countries use of this product is covered by patents. Purchase of product in these countries includes non-transferable, limited license for using only this amount of product for the purchaser's own internal research.

This product is licensed under one or more U.S. Patents Nos. 5,500,363 and 5,352,778 or corresponding foreign patents. This product is licensed under one U.S. Patent No. 5,436,149 or corresponding foreign patents owned by Takara Bio, Inc.

Patent pending.

Product Code. 10679320

Quantity Price
1 £ 864.0 / Pack of 20
EU Stock 20
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Description and Specification

Specification

For Use With (Application) Routine PCR amplification of DNA fragments up to 6kb; RT-PCR; Genotyping; Generation of PCR products for TA cloning
Product Name DreamTaq DNA Polymerase
Quantity 20 x 500U (5U/┬ÁL)
Item Description 5u/uL, 10 x 500U

DreamTaq DNA Polymerase ensures higher sensitivity, longer PCR products and higher yields compared to conventional Taq DNA polymerase. DreamTaq DNA Polymerase uses the same reaction set-up and cycling conditions as conventional Taq DNA polymerase. Extensive optimization of reaction conditions is not required. It is supplied with optimized DreamTaq buffer, which includes 20 mM MgCl2. DreamTaq DNA Polymerase generates PCR products with 3'-dA overhangs. It does not incorporate dUTP.
  • Robust amplification with minimal optimization
  • High yields of PCR products
  • Higher sensitivity compared to conventional Taq DNA polymerase
  • Amplification of long targets up to 6kb from genomic DNA and up to 20kb from viral DNA
  • Generates 3'-dA overhangs
  • Incorporates modified nucleotides

Definition of Activity Unit

  • One unit of the enzyme catalyzes the incorporation of 10nmol of deoxyribonucleotides into a polynucleotide fraction (adsorbed on DE-81) in 30 min at 70°C
  • Enzyme activity is assayed in the following mixture: 67mM Tris-HCl (pH 8.8 at 25°C), 6.7 mM MgCl2, 1mM 2-mercaptoethanol, 50mM NaCl, 0.1mg/mL BSA, 0.75mM activated calf thymus DNA, 0.2mM of each dNTP, 0.4MBq/mL [3H]-dTTP

Storage Buffer

  • The enzyme is supplied in: 20mM Tris-HCl (pH 8.0), 1mM DTT, 0.1mM EDTA, 100mM KCl, stabilizing agent and 50% (v/v) glycerol

Quality Control

  • The absence of endo-, exodeoxyribonucleases and ribonucleases confirmed by appropriate quality tests; Functionally tested in PCR

Inhibition and Inactivation

  • Inhibitors: ionic detergents (deoxycholate, sarkosyl and SDS) at concentrations higher than 0.06, 0.02 and 0.01%, respectively (1)
  • Inactivated by phenol/chloroform extraction

Recommended for:

Routine PCR amplification of DNA fragments up to 6kb; RT-PCR; Genotyping; Generation of PCR products for TA cloning