Human Glypican 3 Alexa Fluor 488 MAb (Clone 307801) 100 TESTS

• Species Reactivity

  Human

• Specificity

  Detects human Glypican 3 in ELISAs and Western blots. Does not cross-react with recombinant human (rh) Glypican 2, rhGlypican 5, or rhGlypican 6.

• Source

  Monoclonal Mouse IgG    _2A Clone # 307801

• Purification

  Protein A or G purified from hybridoma culture supernatant

• Immunogen

  Mouse myeloma cell line NS0-derived recombinant human Glypican 3    
  Gln25-Val558    
  Accession # P51654.1

• Formulation

  Supplied in a saline solution containing BSA and Sodium Azide.

• Label

  Alexa Fluor 488

Applications

• 
  

  Recommended    
  Concentration

  Sample

• Flow Cytometry

  5 µL/10    ⁶ cells

  See below

• 
  

Please Note: Optimal dilutions should be determined by each laboratory for each application.  are available in the Technical Information section on our website.

Data Examples

Preparation and Storage

• Shipping

  The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

• Stability & Storage

  Protect from light.    Do not freeze.    

• 12 months from date of receipt, 2 to 8 °C as supplied.

Background: Glypican 3

Glypicans (GPC) are a family of heparan sulfate proteoglycans that are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor. Six members of this family have been identified in mammals (GPC1-GPC6). All glypican core proteins contain an N-terminal signal peptide, a large globular cysteine-rich domain (CRD) with 14 invariant cysteine residues, a stalk-like region containing the heparan sulfate attachment sites, and a C-terminal GPI attachment site. While glypican proteins do not share strong amino acid sequence identity (they range from 17-63%), the conserved cysteine residues in their CRDs suggests similarity in their three‑dimensional structure (1, 2).

Mutations in GPC3 cause a rare disorder in humans, Simpson-Golabi-Behmel Syndrome, which is characterized by pre and postnatal overgrowth of multiple tissues and organs and an increased risk for developing embryonic tumors (3). These features are also present in the mouse knock-out of GPC3 indicating that GPC3 regulates cell survival and inhibits cell proliferation during development (4). Glypican 3 has been implicated in regulating many different signaling pathways including: IGF, FGF, BMP, and Wnt. An endoproteolytic processing of GPC3 by proprotein convertases is required for the modulation of Wnt signaling (5). Direct interaction with FGF-basic has been observed and is mediated by the heparan sulfate chains (6).

• References:

1. Filmus, J. and S.B. Selleck (2001) J. Clinical Invest. 108:497. 

2. De Cat, B and G. David (2001) Seminars in Cell & Dev. Biol. 12:117. 

3. Pilia, G. et al. (1996) Nat. Genet. 12: 241. 

4. Cano-Gauci, D.F. et al. (1999) J. Cell Biol. 146: 255.

5. De Cat, B. et al. (2003) J. Cell Biol. 163:625.

6. Song, H.H. et al. (1997) J. Biol. Chem. 272:7574.

• Entrez Gene IDs:

  2719 (Human); 14734 (Mouse); 25236 (Rat)

• Alternate Names:

  DGSX; Glypican 3; glypican proteoglycan 3; glypican-3; GPC3; GTR2-2; heparan sulphate proteoglycan; Intestinal protein OCI-5; MXR7; OCI5; OCI-5; secreted glypican-3; SGB; SGBS; SGBS1SDYS