Klenow Fragment
Large fragment of E. coli DNA Polymerase I enzyme which retains both the polymerase and the proofreading 3'→5' exonuclease activities of Polymerase I.
Source
Escherichia coli
Description
- Lacks 5'→3' exonuclease activity (1)
- Ultrapure recombinant enzyme
Fragment Applications
- Used for Sanger dideoxy sequencing (2)
- Suitable for second strand cDNA synthesis (3)
- Used for 3'-end labeling and filling in 5'-protruding sticky ends (4)
Reagents Included
10X DNA Polymerase I (Klenow) Reaction Buffer
Unit Definition
One unit is the amount of enzyme required to incorporate 10 nmoles of total nucleotide into acid insoluble form in 30 minutes at 37°C
Heat Inactivation
75ºC for 15 minutes
Concentration
5 - 10 units/µl
Storage Buffer
50 mM potassium phosphate (pH 7.0)
0.25 mM dithiothreitol
50% (v/v) glycerol
Assay Conditions
67 mM potassium phosphate (pH 7.4)
6.7 mM MgCl2
1 mM dithiothreitol
0.033 mM of each dCTP, dGTP, dTTP and [α-32P]dATP
4.5 µg activated DNA
Incubation for 30 minutes at 37ºC in a total reaction volume of
100 µl
Quality Control
All preparations are assayed for contaminating endonuclease and 5'-exonuclease activities. Typical preparations are greater than 95% pure, as judged by SDS polyacrylamide gel electrophoresis
Storage Conditions
Store at -20°C
Product shipped on dry ice
Certificate of Analysis PDF -Current Lot
MSDS PDF
- Joyce, C.M. and Grindley, N.D., Proc. Natl. Acad. Sci. USA 80, 1830-1834. 1983
- Sanger, F., Nicklen, S. and Coulson, A.R. (1977) Proc. Natl. Acad. Sci. USA 74, 5463-5467
- Houdebine, L.M. (1976) Nucleic Acids Res. 3, 615-630
- Sambrook, J., Fritsch, E.F., and Maniatis, T. (1989) Mol. Cloning: A Laboratory Manual, Second Ed. pp. 5.34, 5,4-5.43
- Richardson, C.C.. Schildkraut, C.L., Aposhian, H.V. and Kornberg, A., J. Biol. Chem. 239, 222-232. 1964