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UMOD Polyclonal Antibody

规格: / 50μL / 100μL
价格: / ¥1010 / ¥1640

货号:D-AB-10364L

货期:咨询

宿主: Rabbit

反应性: H

应用: IHC

  • 详情
  • Overview

    Synonyms ADMCKD2,FJHN,HNFJ,HNFJ1,MCKD2,medullary cystic kidney disease 2 (autosomal dominant),Tamm Horsfall glycoprotein,Tamm Horsfall urinary glycoprotein,Tamm-Horsfall urinary glycoprotein,THGP,THP,Umod,Urehd1,urehr4,UROM_HUMAN,uromodulin (uromucoid, Tamm-Horsfall glycoprotein), Uromodulin
    Swissprot P07911
    Source Rabbit
    Reactivity Human
    Immunogen Recombinant Human UMOD protein expressed by E.coli
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:100-1:200
    Concentration 1mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cell membrane. Secreted.
    Tissue specificity Synthesized by kidney. Most abundant protein in normal human urine.
    Isotype IgG
    Purification Antigen Affinity Purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide,1% protective protein and 50% glycerol,pH7.4
    Background The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. 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. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants.
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