UMOD polyclonal antibody

Catalog # PAB15392

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Size:2 mL
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Goat polyclonal antibody raised against UMOD.

    Immunogen

    Human UMOD.

    Host

    Goat

    Reactivity

    Human

    Specificity

    This product is suitable for use as a precipitating antibody. Cross-reactivity to other species may exist. Antibody activity to other serum proteins is not present.

    Form

    Lyophilized

    Recommend Usage

    ELISA (1:400-1:2000)
    Immunohistochemistry (1:50-1:200)
    Western Blot (1:100-1:500)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    Lyophilized from 20 mM sodium phosphate buffer, 140 mM NaCl, pH 7.3 (0.05% sodium azide).

    Storage Instruction

    Store at 4°C on dry atmosphere.
    After reconstitution with 2 mL of deionized water, store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot

    Enzyme-linked Immunoabsorbent Assay

    Immunodiffusion

  • 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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