UMOD (Human) Matched Antibody Pair

Catalog # H00007369-AP51

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Size:1 Set
Price: USD $ 607.00
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QC Test

Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the UMOD 293T overexpression lysate (non-denatured).

  • Specification

    Product Description

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

    Reactivity

    Human

    Quality Control Testing

    Standard curve using UMOD 293T overexpression lysate (non-denatured) as an analyte.

    Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the UMOD 293T overexpression lysate (non-denatured).

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: mouse monoclonal anti-UMOD (100 ug)
    2. Detection antibody: rabbit purified polyclonal anti-UMOD (50 ug)
    *Reagents are sufficient for at least 3-5 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 (Transfected lysate)

  • Gene Info — UMOD

    Entrez GeneID

    7369

    Gene Name

    UMOD

    Gene Alias

    ADMCKD2, FJHN, HNFJ, MCKD2, THGP, THP

    Gene Description

    uromodulin

    Omim ID

    162000 191845 603860 609886

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes uromodulin, the most abundant protein in normal urine. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. Uromodulin may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of uromodulin in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the autosomal dominant renal disorders medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure. 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

    OTTHUMP00000162212|Tamm-Horsfall glycoprotein|uromodulin (uromucoid, Tamm-Horsfall glycoprotein)|uromucoid

  • 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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