DNA Polymerase (Highly Pure)


Catalog Number: B2012511 (0.1 mg)
DNA Polymerase (Highly Pure) is a high quality enzyme that catalyzes the formation of DNA molecules from nucleoside triphosphates. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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SKU: B2012511 Categories: , Tag:


DNA Polymerase (Highly Pure)
Catalog number: B2012511
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 0.1 mg
Molecular Weight or Concentration: N/A
Supplied as: Liquid
Applications: molecular tool for various biochemical applications
Storage: -20°C
Keywords: DNAP
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

1: Hager DA, Jin DJ, Burgess RR. Use of Mono Q high-resolution ion-exchange chromatography to obtain highly pure and active Escherichia coli RNA polymerase Biochemistry. 1990 Aug 28;29(34):7890-4.
2: Eckert KA, Hile SE. Every microsatellite is different: Intrinsic DNA features dictate mutagenesis of common microsatellites present in the human genome Mol Carcinog. 2009 Apr;48(4):379-88.
3: Marcone C. Comparison of Different Procedures for DNA Extraction for Routine Diagnosis of Phytoplasmas Methods Mol Biol. 2019;1875:71-81.
4: Otaño-Rivera V, Boakye A, Grobe N, Almutairi MM, Kursan S, Mattis LK, Castrop H, Gurley SB, Elased KM, Boivin GP, Di Fulvio M. A highly efficient strategy to determine genotypes of genetically-engineered mice using genomic DNA purified from hair roots Lab Anim. 2017 Apr;51(2):138-146.
5: Slaby I, Holmgren A. Rapid isolation of homogeneous cloned T7 gene 5 protein and T7 DNA polymerase by affinity chromatography on immobilized thioredoxin Protein Expr Purif. 1991 Aug;2(4):270-7.
6: Yu X, Seitz S, Pointon T, Bowlin JL, Cohrs RJ, Jonjić S, Haas J, Wellish M, Gilden D. Varicella zoster virus infection of highly pure terminally differentiated human neurons J Neurovirol. 2013 Feb;19(1):75-81.
7: Griep MA. Primase structure and function Indian J Biochem Biophys. 1995 Aug;32(4):171-8.
8: Bhadra S, Paik I, Torres JA, Fadanka S, Gandini C, Akligoh H, Molloy J, Ellington AD. Preparation and Use of Cellular Reagents: A Low-resource Molecular Biology Reagent Platform Curr Protoc. 2022 Mar;2(3):e387.
9: Mygind T, Østergaard L, Birkelund S, Lindholt JS, Christiansen G. Evaluation of five DNA extraction methods for purification of DNA from atherosclerotic tissue and estimation of prevalence of Chlamydia pneumoniae in tissue from a Danish population undergoing vascular repair BMC Microbiol. 2003 Sep 2;3:19.
10: Niessen L. Loop-mediated isothermal amplification-based detection of Fusarium graminearum Methods Mol Biol. 2013;968:177-93.

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