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GBA Polyclonal Antibody

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

货号:E-AB-19899

宿主: Rabbit

反应性: H,M

应用: WB,IHC

  • 详情
  • Overview

    Synonyms Acid beta glucosidase,Acid beta-glucosidase,Alglucerase,Beta glucocerebrosidase,BETA GLUCOSIDASE, ACID,Beta-glucocerebrosidase,betaGC,D glucosyl N acylsphingosine glucohydrolase,D-glucosyl-N-acylsphingosine glucohydrolase,EC 3.2.1.45 ,GBA,Gba protein ,GBA1,GC,GCase,GCB,GLCM,GLUC,Glucocerebrosidase (alt.) ,Glucocerebrosidase,GLUCOCEREBROSIDASE PSEUDOGENE,Glucosidase beta,Glucosidase, beta, acid,Glucosidase, beta; acid (includes glucosylceramidase),Glucosylceramidase,Imiglucerase,Lysosomal glucocerebrosidase ,OTTHUMP00000033992,OTTHUMP00000033993,GBA抗体
    Swissprot P04062
    Source Rabbit
    Reactivity Human, Mouse
    Immunogen Synthetic peptide of human GBA
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:50-1:100;
    Concentration 1.56mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Lysosome membrane. Interaction with saposin-C promotes membrane association.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4
    Background This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.
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