RNASEH2A (Human) Matched Antibody Pair

Catalog # H00010535-AP11

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Price

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Quantity

Size:1 Set
Price: USD $ 607.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human RNASEH2A.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Rat (84)

    Quality Control Testing

    Standard curve using recombinant protein ( H00010535-P01 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-RNASEH2A (100 ug)
    2. Detection antibody: mouse monoclonal anti-RNASEH2A, IgG1 Kappa (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — RNASEH2A

    Entrez GeneID

    10535

    Gene Name

    RNASEH2A

    Gene Alias

    AGS4, JUNB, RNASEHI, RNHIA, RNHL

    Gene Description

    ribonuclease H2, subunit A

    Omim ID

    606034 610333

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a component of the heterotrimeric type II ribonuclease H enzyme (RNAseH2). RNAseH2 is the major source of ribonuclease H activity in mammalian cells and endonucleolytically cleaves ribonucleotides. It is predicted to remove Okazaki fragment RNA primers during lagging strand DNA synthesis and to excise single ribonucleotides from DNA-DNA duplexes. Mutations in this gene cause Aicardi-Goutieres Syndrome (AGS), a an autosomal recessive neurological disorder characterized by progressive microcephaly and psychomotor retardation, intracranial calcifications, elevated levels of interferon-alpha and white blood cells in the cerebrospinal fluid

    Other Designations

    ribonuclease H2, large subunit|ribonuclease HI, large subunit

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