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IHC-P analysis of human hepatocellular carcinoma tissue section using GTX03328 Glypican-3 antibody [YP7].
IHC-P analysis of human hepatocellular carcinoma tissue section using GTX03328 Glypican-3 antibody [YP7].
IHC-P analysis of human hepatocellular carcinoma tissue section using GTX03328 Glypican-3 antibody [YP7].

Glypican-3 antibody [YP7]

Research Use Only
GTX03328
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetGPC3
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Overview

  • Supplier
    GeneTex
  • Product Name
    Glypican-3 antibody [YP7]
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:25-1:50. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    YP7
  • Conjugate
    Unconjugated
  • Formulation
    Liquid
  • Gene ID2719
  • Target name
    GPC3
  • Target description
    glypican 3
  • Target synonyms
    DGSX; glypican proteoglycan 3; glypican-3; GTR2-2; heparan sulphate proteoglycan; intestinal protein OCI-5; MXR7; OCI-5; SDYS; secreted glypican-3; SGB; SGBS; SGBS1
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP51654
  • Protein Name
    Glypican-3
  • Scientific Description
    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. [provided by RefSeq, Sep 2009]
  • Reactivity
    Human
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203