HGF R/c-MET Antibody Summary
Recombinant mouse hepatocyte growth factor receptor (HGF R) extracellulardomain expressed in Sf 21 cells.
Cell Membrane
Anti-Human HGF will neutralize the biological activity of rhHGF. The antibody may also be used in immunoblotting and ELISA. By ELISA, the shows approximately 15% cross-reactivity with recombinant human HGF receptor and no cross-reactivity with recombinant human macrophage stimulating protein receptor.
IgG
Polyclonal
Goat
MET
Immunogen affinity purified
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Applications/Dilutions
- Western Blot 0.1-0.2 ug/ml
- Blocking/Neutralizing 0.3-1 ug/ml
- ELISA .5-1 ug/ml
ELISA: The detection limit for recombinant mouse HGF R is approximately 0.3 ng/well. WB: The detection limit for recombinant mouse HGF R is approximately 25 ng/lane under non-reducing and reducing conditions. Predicted molecular weight: 87 kDa.Anti-Mouse Hepatocyte Growth Factor Receptor has the ability to neutralize receptor-ligand interaction. Approximately 0.3-1.0 ug/ml of the antibody will block 50% of the binding of recombinant human HGF (5 ng/ml) to immobilized recombinant mouse HGF R/Fc chimera (100 ul of a 1 ug/ml solution coated in each well) in an ELISA.
Reactivity Notes
Expected to cross-react with Mouse (89% identity with immunogen) due to sequence homology. Not yet tested in other species.
Packaging, Storage & Formulations
Store at -20C. Avoid freeze-thaw cycles.
PBS and 5% Trehalose
No Preservative
0.1 mg/ml
Immunogen affinity purified
Alternate Names for HGF R/c-MET Antibody
- AUTS9
- cMET
- c-MET
- EC 2.7.10
- EC 2.7.10.1
- hepatocyte growth factor receptor
- HGF R
- HGF receptor
- HGF/SF receptor
- HGFR
- Met (c-Met)
- met proto-oncogene (hepatocyte growth factor receptor)
- met proto-oncogene tyrosine kinase
- MET
- oncogene MET
- Proto-oncogene c-Met
- RCCP2
- Scatter factor receptor
- SF receptor
- Tyrosine-protein kinase Met
Background
Hepatocyte growth factor receptor (HGF R), a product of the proto-oncogene c-Met, is a heterodimeric transmembrane glycoprotein that is a receptor-type tyrosine kinase. The c-Met heterodimer is composed of an alpha chain that is disulfide-linked to a beta chain. Each alpha and beta subunit heterodimer contain 1152 amino acid residues with a calculated molecular mass of approximately 129 kDa. The alpha chain is exposed to the cell surface and the beta chain spans the plasma membrane. c-Met is synthesized as a single-chain precursor which undergoes cotranslational glycosylation and proteolytic cleavage producing the heterodimeric mature form. Human and mouse HGF receptors share 89% amino acid identity. HGF is the ligand for the HGF receptor. Human HGF can bind to the mouse HGF receptor.Hepatocyte growth factor (HGF), also known as scatter factor (SF), is a multifunctional cytokine that promotes mitogenesis, migration, invasion, and morphogenesis. HGF stimulates hepatocytes and other epithelial and endothelial cells by various biological actions. HGF binding involves the beta chain of the HGF receptor, but alpha chain participation cannot be ruled out. HGF binding to c-Met triggers dimerization and subsequent tyrosine autophosphorylation of the receptor beta chain. Autophophorylation at two tyrosines upregulates kinase activity while phosphorylation at two other tyrosines generates SH2 docking sites for adapter proteins such as Shc, Grb2, CrK/CRKL, and Gab1. Receptor activation has been correlated to the activation of the Ras pathway, which culminates in the activation and consequent nuclear translocation of MAP kinase. c-Met can also be negatively modulated by phosphorylation of Ser 985 by protein kinase C. Other ligand-receptor activities involve binding that leads to enhanced integrin-mediated B cell and lymphoma cell adhesion. Normal HGF-Met signaling is needed for embryonic development and abnormal signaling and has been implicated in tumorigenesis.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
product targets : JAK/STAT_Compound_Library inhibitors