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GPC3 Polyclonal Antibody

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

货号:E-AB-53438

宿主: Rabbit

反应性: H,M

应用: IHC

  • 详情
  • Overview

    Synonyms DGSX,Glypican proteoglycan 3,Glypican-3 [Precursor],Gpc3,GPC3,GTR2 2,GTR2-2,Heparan sulphate proteoglycan,Intestinal protein OCI 5,Intestinal protein OCI-5,MXR7,OCI 5,OCI-5,OCI5,SDYS,Secreted glypican-3,SGB,SGBS,SGBS1,GPC3抗体
    Swissprot P51654
    Source Rabbit
    Reactivity Human, Mouse
    Immunogen Synthetic peptide of human GPC3
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:40-1:200
    Concentration 1.8mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cell membrane and Secreted>extracellular space.
    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 Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants.
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