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Purified anti-c-Met Antibody

Pricing & Availability
Clone
12.1 (See other available formats)
Regulatory Status
RUO
Other Names
MET, Hepatocyte growth factor receptor, HGF receptor
Isotype
Mouse IgG1, κ
Ave. Rating
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Product Citations
publications
12dot1_PURE_c-Met_Antibody_WB_110617
Total lysates (10 µg protein) from HeLa and HeLa c-Met knockout (KO) cells were resolved by electrophoresis (4-20% Tris-glycine gel), transferred to nitrocellulose, and probed with 1:250 (2 µg/ml) purified anti- c-Met antibody , clone 12.1 (upper). Proteins were visualized using chemiluminescence detection by incubation with HRP goat anti-mouse-IgG secondary antibody (cat#405306). Direct-Blot™ HRP anti-&beta:-actin Antibody (Cat#643807) was used as a loading control (lower). Lane M is the Moleculuar weight ladder.
  • 12dot1_PURE_c-Met_Antibody_WB_110617
    Total lysates (10 µg protein) from HeLa and HeLa c-Met knockout (KO) cells were resolved by electrophoresis (4-20% Tris-glycine gel), transferred to nitrocellulose, and probed with 1:250 (2 µg/ml) purified anti- c-Met antibody , clone 12.1 (upper). Proteins were visualized using chemiluminescence detection by incubation with HRP goat anti-mouse-IgG secondary antibody (cat#405306). Direct-Blot™ HRP anti-&beta:-actin Antibody (Cat#643807) was used as a loading control (lower). Lane M is the Moleculuar weight ladder.
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689902 100 µg £174
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Description

The Mesenchymal Epithelial Transition (MET) receptor belongs to a family of Receptor tyrosine kinases (RTKs). The MET proto-oncogene is located on chromosome 7q21–31 and encodes the receptor tyrosine kinase C-Met. It  is a 190 kD glycoprotein heterodimer made up of an extracellular α-chain which is linked by a disulphide bond to a transmembrane β-chain. c-Met is initially synthesised as a 170 kD single polypeptide as precursor that is proteolytically cleaved to form the α-chain and the β-chain. TPR-MET oncogenic fusion protein from human osteosarcoma tumor cells was first discovered in 1984. c-Met is a hepatocyte growth factor (HGF) receptor. The initiation of MET signaling begins with the binding of HGF to the MET receptor at cell membrane that causes C-Met dimerization. Subsequent activation is through a process of trans-phosphorylation of the two tyrosine residues in the catalytical regions Y1234 and Y1235, followed by trans-phosphorylation of two docking tyrosines (Y1349 and Y1356). It enables MET to bind to multiple substrates and activate a variety of signaling pathways, such as MAPK, PI3K-AKT cascades, STAT and NF-κB signaling pathways. This is responsible for driving proliferation, cell survival, migration and invasiveness. c-Met is overexpressed in different human tumors, such as thyroid, gastric, pancreatic, breast, cervical and prostate cancers. Increasing evidence indicated that MET may be a common mechanism of resistance to anticancer treatment such as approved EGFR and VEGFR inhibitors, anti-HER2 therapies and a BRAF inhibitor. Hence, the HGF-MET axis has been targeted  in solid tumors to overcome the drug resistance.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Human
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
Bacterially expressed human c-Met alpha chain.
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

WB - Quality tested
KO/KD-WB - Verified
Recommended Usage

Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 0.5 - 2.5 µg per ml. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

Clone 12.1 does not cross-react with mouse. Clone 12.1 recognizes the precursor and a chain c-Met; the ß chain will not be recognized by this antibody.

RRID
AB_2629791 (BioLegend Cat. No. 689902)

Antigen Details

Structure
Heterodimer made of an alpha chain (50 kD) and a beta chain (145 kD) which are disulfide linked.
Distribution

Membrane; single-pass type I membrane protein.

Function
Receptor tyrosine kinase that transduces signals from the extracellular matrix into the cytoplasm by binding to hepatocyte growth factor/HGF ligand. Regulates many physiological processes including proliferation, scattering, morphogenesis and survival.
Interaction
Interacts with SPSB1, SPSB2, SPSB3, SPSB4, INPP5D/SHIP1, RANBP9, RANBP10, MUC20, GRB10, PTPN1 and PTPN2. When phosphorylated, interacts with STAT3, PIK3R1, SRC, PCLG1, GRB2, GAB1 and INPPL1/SHIP2.
Ligand/Receptor
HGF.
Biology Area
Cancer Biomarkers, Cell Biology, Cell Proliferation and Viability, Signal Transduction
Molecular Family
Protein Kinases/Phosphatase
Antigen References

1. Garajová I, et al. 2015. Transl. Oncogenomics 7:13.
2. Cooper CS, et al. 1984. Nature. 311:29.
3. Furge KA, et al. 2000. Oncogene. 19:5582.
4. Ponzetto C, et al. 1994. Cell. 77(2):261-71.

Gene ID
4233 View all products for this Gene ID
UniProt
View information about c-Met on UniProt.org
Go To Top Version: 1    Revision Date: 08/31/2016

For Research Use Only. Not for diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
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