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FIGURE: 1 / 6
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total GPC3.
GPC3 is a cell surface proteoglycan that bears heparan sulfate. This protein may be involved in the suppression/modulation of growth in the predominantly mesodermal tissues and organs, and may play a role in the modulation of IGF2 interactions with its receptor and thereby modulate its function. Members of the glypican-related integral membrane proteoglycan family contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol (GPI) linkage. These proteins may play a role in the control of cell division, growth regulation, and tumor predisposition. Deletion mutations in GPC3 are the cause of Simpson-Golabi-Behmel syndrome (SGBS), also known as Simpson dysmorphia syndrome (SDYS). SGBS is a condition characterized by pre- and postnatal overgrowth (gigantism) with visceral and skeletal anomalies.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: cell surface protein; precursor core protein cleaved by furin; defective in Simpson-Golabi-Behmel overgrowth syndrome; glypican proteoglycan 3; GTR2-2; GTR22; heparan sulphate proteoglycan; intestinal protein OCI-5; OCI-5; proteoglycan GPC3; secreted glypican-3; unnamed protein product
Gene Aliases: DGSX; GTR2-2; MXR7; OCI-5; SDYS; SGB; SGBS; SGBS1
UniProt ID: (Human) P51654, (Mouse) Q8CFZ4, (Rat) P13265
Entrez Gene ID: (Human) 2719, (Mouse) 14734, (Rat) 25236
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