DNA Polymerase I Large (Klenow) Fragment

by Promega
Available SKUs: M2201 | M2206 |
Login to view price.

Description

  • Overview
  • Protocols
  • Specifications
  • Resources
  • DNA Polymerase I Large (Klenow) Fragment is a 68kDa C-terminal fragment of E. coli DNA Polymerase I that lacks the 5´?3´ exonuclease activity of intact DNA polymerase I but retains its 5´?3´ polymerase, 3´?5´ exonuclease and strand displacement activities. The 5´?3´ polymerase activity of Klenow Fragment can be used to fill in 5´-protruding ends with unlabeled or labeled dNTPs, to sequence single- or double-stranded DNA templates, for in vitro mutagenesis using synthetic oligonucleotides, for cDNA second-strand synthesis and to generate single-stranded DNA probes. The 3´?5´ exonuclease activity can be used to generate blunt ends from a 3´-overhang. The DNA-dependent DNA polymerase is provided with 10X Reaction Buffer [500mM Tris-HCl (pH 7.2 at 25°C), 100mM MgSO4, 1mM DTT].

    Choose Your Configuration: Learn more about our custom options for this product at: www.promega.com/custom/

    References

    1. Anderson, S. et al. (1980) Nucl. Acids Res. 8, 1731–43.
    2. Sanger, F. et al. (1977) Proc. Natl. Acad. Sci. USA 74, 5463–7.
    3. Wallace, R.B. et al. (1980) Science 209, 1396–400.
    4. Houdebine, L.M. (1976) Nucl. Acids Res. 3, 615–30.
    5. Feinberg, A.P. and Vogelstein, B. (1983) Anal. Biochem. 132, 6–13.
    6. Tabor, S. and Struhl, K. (1987) In: Current Protocols in Molecular Biology, Ausubel, F.M. et al., eds., John Wiley and Sons, New York, NY.
    7. Joyce, C.M. and Grindley, N.D.F. (1983) Proc. Natl. Acad. Sci. USA 80, 1830–4.

    Storage Buffer: 50mM Tris-HCl (pH 7.5), 1mM DTT, 0.1mM EDTA and 50% (v/v) glycerol.

    Source: Recombinant E. coli strain.

    QC Tests: Activity, SDS-PAGE/purity, endonuclease.

    Unit Definition: One unit is defined as the amount of enzyme that incorporates 10nmol of total deoxyribonucleotides into TCA-insoluble material in 30 minutes at 37°C. The reaction conditions are: 67mM potassium phosphate (pH 7.5 at 25°C), 6.7mM MgCl2, 1mM DTT, 50ug/ml activated calf thymus DNA and 33uM each of dATP, dCTP, dGTP and dTTP (a mix of unlabeled and [3H]dTTP).

  • Protocols

    Complete Protocol

    Download PDF

    DNA Polymerase I Large (Klenow) Fragment Protocol

    PDF (112 KB)

  • Certificate of Analysis

    Lookup Certificate of Analysis

    Storage Conditions

    -30C TO -10C

    Use Restrictions

    For Research Use Only. Not for Use in Diagnostic Procedures.

  • Resources

    Citations

You recently viewed

Clear recently viewed