TDP1 (Human) ELISA Kit

Catalog # KA6122

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Size:1 Kit
Price: USD $ 648.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.

  • Specification

    Product Description

    TDP1 (Human) ELISA Kit is a sandwich enzyme-linked immunosorbent assay for quantitative detection of human TDP1 in Serum, Plasma and Cell Culture.

    Suitable Sample

    Serum, Plasma, Cell Culture

    Sample Volume

    50 uL

    Label

    Peroxidase-conjugated

    Detection Method

    Colorimetric

    Assay Type

    Quantitative

    Calibration Range

    1.563 to 100 ng/mL

    Reactivity

    Human

    Regulatory Status

    For research use only (RUO)

    Quality Control Testing

    Standard curve

    The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.

    Storage Instruction

    Store components of the kit at 4°C or -20°C as described in the protocol.

  • Applications

    Quantification

  • Gene Info — TDP1

    Entrez GeneID

    55775

    Protein Accession#

    Q9NUW8

    Gene Name

    TDP1

    Gene Alias

    FLJ11090, MGC104252

    Gene Description

    tyrosyl-DNA phosphodiesterase 1

    Omim ID

    607198 607250

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene 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. This protein 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. This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains. Mutations in this gene are associated with the disease spinocerebellar ataxia with axonal neuropathy (SCAN1). While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform. [provided by RefSeq

    Other Designations

    -

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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