SKU: WM1740 Categories: ,

Glypican-3 [ABT068] mouse mAb

Price range: $268.00 through $328.00

SKU: WM1740-50
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Product details

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. [provided by RefSeq, Sep 2009],

Specifications

Size50μL/100μL
TargetGlypican-3
ReactivityHuman
ApplicationsIHC, ELISA
MW(Calculated)66kD
MW(Observed)58kD
Host SpeciesMouse
IsotypeIgG1,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:50-200; ELISA 1:500-5000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationThe antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRMM068
ImmunogenSynthesized peptide derived from human Glypican-3(GPC3) AA range: 400-500
SpecificityThe antibody can specifically recognize human Glypican-3 protein.
Gene NameGPC3 OCI5
Protein NameGlypican-3(GPC3)
Other NameGlypican-3; / GTR2-2; / Intestinal protein OCI-5; / MXR7; / [Cleaved into: Secreted glypican-3]
SpeciesHuman
Gene ID2719
UniprotP51654
Species.1
Gene ID.1
Uniprot.1
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationCytoplasmic
Tissue ExpressionHighly expressed in lung, liver and kidney.
Signaling_pathway
Research Areas>>Proteoglycans in cancer
FunctionDisease:Defects in GPC3 are the cause of Simpson-Golabi-Behmel syndrome (SGBS) [MIM:312870]; also known as Simpson dysmorphia syndrome (SDYS). SGBS is a condition characterized by pre- and postnatal overgrowth (gigantism) with visceral and skeletal anomalies.,Function:Cell surface proteoglycan that bears heparan sulfate.,Function:Cell surface proteoglycan that bears heparan sulfate. May be involved in the suppression/modulation of growth in the predominantly mesodermal tissues and organs. May play a role in the modulation of IGF2 interactions with its receptor and thereby modulate its function. May regulate growth and tumor predisposition.,similarity:Belongs to the glypican family.,tissue specificity:Highly expressed in lung, liver and kidney.,
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