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ASAH1 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-10959

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC,ELISA

  • 详情
  • 文献(3)
  • Overview

    Synonyms AC,ACDase,Acid CDase,Acid ceramidase,Acid ceramidase precursor,Acid ceramidase subunit beta,Acylsphingosine deacylase,ASAH 1,ASAH,ASAH1,ASAH1,FLJ21558,FLJ22079,N acylsphingosine amidohydrolase (acid ceramidase) 1,N acylsphingosine amidohydrolase 1,N acylsphingosine amidohydrolase,N-acylsphingosine amidohydrolase,N-acylsphingosine deacylase,PHP,PHP32,Putative 32 kDa heart protein,SMAPME,ASAH1抗体
    Swissprot Q13510
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant protein of human ASAH1
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213),ELISA
    Recommended dilution WB 1:1000-1:5000, IHC 1:50-1:200
    Concentration 0.4 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Lysosome.
    Tissue specificity Broadly expressed with highest expression in heart.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background This gene encodes a heterodimeric protein consisting of a nonglycosylated alpha subunit and a glycosylated beta subunit that is cleaved to the mature enzyme posttranslationally. The encoded protein catalyzes the synthesis and degradation of ceramide into sphingosine and fatty acid. Mutations in this gene have been associated with a lysosomal storage disorder known as Farber disease. Multiple transcript variants encoding several distinct isoforms have been identified for this gene.
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