TDP1 Human, Sf9

SKU:BHZ11000153
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    Overview
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    Tyrosyl-DNA Phosphodiesterase 1 Human Recombinant, Sf9 TDP1 belongs to the phospholipase D family and contains two PLD phosphodiesterase domains. TDP1 is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. TDP1 may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. Mutations in the TDP1 gene are linked to the disease spinocerebellar ataxia with axonal neuropathy (SCAN1).
    Enzyme Type Tyrosine Kinase
    Species Human
    Form Liquid
    Expression System Sf9 Insect Cells
    Purity 90.0%
    Gene Symbol TDP1, Sf9
    Source Sf9, Baculovirus cells.
    Available Options
    1µg | 5µg | 50µg
    Options selector
    Catalog no. Size
    ENZ-1038-1µg 1µg
    ENZ-1038-5µg 5µg
    ENZ-1038-50µg 50µg
    Field Specification
    Enzyme Type
    • Tyrosine Kinase
    Expression System
    • Sf9 Insect Cells
    Form Liquid
    Formulation TDP1 protein solution (0.25mg/ml) containing Phosphate Buffered Saline (pH 7.4) and 10% glycerol.
    Product Type
    • Enzyme
    Purity 90.0%
    Source Sf9, Baculovirus cells.
    Species Human
    Storage Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles.
    Target TDP1, Sf9

    Product Description

    Tyrosyl-DNA Phosphodiesterase 1 Human Recombinant, Sf9

    Overview

    TDP1 belongs to the phospholipase D family and contains two PLD phosphodiesterase domains. TDP1 is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. TDP1 may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. Mutations in the TDP1 gene are linked to the disease spinocerebellar ataxia with axonal neuropathy (SCAN1).

    Specifications

    Purity Greater than 90.0% as determined by SDS-PAGE.
    Formulation TDP1 protein solution (0.25mg/ml) containing Phosphate Buffered Saline (pH 7.4) and 10% glycerol.
    Storage Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles.
    Expression System Sf9, Baculovirus cells.

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