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DNA Polymerase I Klenow Fragment exo-

Cat# DIA-583
Source Escherichia coli
Description This N-terminally truncated form of DNA polymerase I retains DNA polymerase activity but lacks 5′→3′ exonuclease activity. Additional mutations (D355A, E357A) eliminate its 3′→5′ exonuclease activity.
As a result, the enzyme provides polymerase activity without proofreading, making it suitable for applications requiring controlled nucleotide incorporation.
Unit Definition One unit is defined as the amount of enzyme required to incorporate 10 nmol of dNTP into acid-insoluble material within 30 minutes at 37 °C.
Storage -20 °C
Buffer 25 mM Tris-HCl pH 7.4,  0.1 mM EDTA,  1 mM DTT,  50% glycerol
Applications Dideoxy sequencing; random primer labeling; 3′ dA-tailing during library preparation.
Product Overview 3′ dA-tailing.
Probe preparation using random primers.
Random primer labeling.
Package 5000 U
Klenow Fragment exo- (5 U/μL): 1 mL
10× Blue Buffer (100 mM Tris-HCl pH 7.9, 500 mM NaCl, 100 mM MgCl2, 10 mM DTT): 2 mL
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