Keep as concentrated solution.
Positive Control: HepG2, HepG2 (24 µg/ml Tunicamycin treatment for 16 hr).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial. For short-term storage (1-2 weeks), product can be stored at 4°C. For long-term storage, aliquot and store product at -20° C or below, avioiding multiple freeze-thaw cycles.
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: DGSX antibody; glypican 3 antibody; glypican proteoglycan 3; Glypican-3; Glypican-3 alpha subunit; Glypican-3 antibody; Glypican-3 antibody [GT2473] antibody; Glypican-3 beta subunit; GPC3 antibody; GTR2-2; GTR22 antibody; heparan sulphate proteoglycan; Intestinal protein OCI-5; MXR7; MXR7 antibody; OCI5 antibody; SDYS antibody; secreted glypican-3; SGB antibody; SGBS antibody; SGBS1 antibody
Gene Aliases: DGSX; GPC3; GTR2-2; MXR7; OCI-5; OCI5; SDYS; SGB; SGBS; SGBS1
UniProt ID: (Human) P51654
Entrez Gene ID: (Human) 2719