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T4 DNA Polymerase (500u)

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M4215

Description

T4 DNA Polymerase catalyzes the 5´→3´ synthesis of DNA from a primed single-stranded DNA template. Although possessing a potent 3´→5´ proofreading exonuclease, T4 DNA Polymerase contains no 5´→3´ exonuclease activity. T4 DNA Polymerase can be used to fill 5´ protruding ends with labeled or unlabeled dNTPs or for the generation of blunt ends from DNA molecules with 3´ overhangs.

Features - Benefits

  • High Fidelity: T4 DNA Polymerase is the enzyme of choice for applications where misincorporation is a concern.
  • Flexible: T4 DNA Polymerase may be used in a variety of molecular applications. Active in many Promega 1X restriction enzyme buffers.
  • May Be Heat-Inactivated: T4 DNA Polymerase is inactivated by heating at 75°C for 10 minutes.
  • Provided with 10X Reaction Buffer: 250mM Tris-acetate (pH 7.7), 1M potassium acetate, 100mM magnesium acetate and 10mM DTT.
  • Choose Your Configuration: Learn more about our custom options for this product at: www.promega.com/custom/

Applications

  • Flush 5´ protruding ends with labeled or unlabeled dNTPs.
  • Blunt 3´ overhangs.
  • In vitro mutagenesis.

References

  1. Challberg, M.D. and Englund, P.T. (1980) Meth. Enzymol. 65, 39–43.
  2. Burd, J.F. and Wells, R.D. (1974) J. Biol. Chem. 249, 7094–801.
  3. Kunkel, T.A., Loeb, L.A. and Goodman, M.F. (1984) J. Biol. Chem. 259, 1539–45.

Specifications

QC Tests

Activity, SDS-PAGE/purity, endonuclease.

Source

Recombinant E. coli strain.

Storage Buffer

200mM potassium phosphate (pH 6.5 at 25°C), 2mM DTT and 50% glycerol.

Storage Conditions

Store at –20°C.

Unit Definition

One unit is defined as the amount of enzyme required to catalyze the incorporation of 55nmol of dTTP into acid-precipitable material in 30 minutes at 39°C using poly(dA):oligo(dT) as a substrate.

For product intended use please see Patents & Disclaimers tab.

Related citations

Resources

Use Restrictions

M4211, M4215 For Research Use Only. Not for Use in Diagnostic Procedures.

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