DNA POLYMERASE I

PRODUCTS

DNA Polymerase I Highlights

DNA Polymerase I is a mesophilic E. coli polymerase that catalyzes 5′ → 3′ template-directed DNA synthesis. DNA Polymerase I has 3′ → 5′ exonuclease (proofreading) activity and 5′ → 3′ exonuclease activity. It is capable of catalyzing de novo synthesis of synthetic homopolymers and provides a convenient method for the preparation of a variety of defined DNA substrates in the laboratory.

  • Effective nick translation
  • Reduce material costs with a drop-in solution that delivers equivalent performance at a differentiated price-point
  • Custom formats, including high concentration, support lyophilization applications
  • Highly stringent enzyme manufacturing ensures quality performance across lots

Applications

  • Nick translation
  • Second-strand synthesis

ALSO AVAILABLE

High-purity T4 DNA Ligase

Available with standard and rapid ligation buffers for simple optimization

LEARN MORE

For assay developers – make realizing your next product easier
  • Navigate the complexities of productization with an experienced team who’s as committed to your success as you are
  • All aspects of our customization process are designed to serve you with speed, agility, and above all else, a commitment to quality
  • Tailored fill volumes, labeling (including white and private label), and packaging designed to your specifications
  • All products are manufactured within an ISO 13485:2016-certified QMS (download our certificate)
QC Specifications
Description Specification
Protein Purity Assay ≥ 99%
Endonuclease Contamination Assay* Not detectable
DNA contamination Assay (E. coli, mammalian, library)* < 10 copies
Phosphatase Contamination Assay* < 1% released
Unit Assay* Pass

*As assessed using 2 U of enzyme input per assay.

Properties

Unit definition: One unit is defined as the amount of DNA Polymerase I that will incorporate 300 nmol of dNTPs into a DNA template in 60 minutes at 37°C

Reaction conditions (materials not included in the kit):
50 mM Tris-HCl, pH 7.9
10 mM MgCl₂
1 mM DTT

Storage buffer: 25 mM Tris-HCl, pH 7.4, 0.1 mM EDTA, 50% Glycerol, 1 mM DTT

Heat inactivation: 75°C for 20 min

Molecular weight: 103 kDa

5′ – 3′ Exonuclease Activity: Yes
3′ – 5′ Exonuclease Activity: Yes
Strand Displacement Activity: No
Fidelity: High
Processivity: Moderate