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SDS-PAGE

c-MET / HGFR recombinant protein

Recombinant Mouse c-MET / HGFR Protein (Fc tag) (Fc tag)

Gene Names
Met; HGF; HGFR; Par4; c-Met; AI838057
Purity
> 92 % as determined by SDS-PAGE
Synonyms
c-MET / HGFR; Recombinant Mouse c-MET / HGFR Protein (Fc tag) (Fc tag); AI838057; HGF; HGFR; Par4; c-Met; c-MET / HGFR recombinant protein
Ordering
For Research Use Only!
Host
Human Cells
Purity/Purification
> 92 % as determined by SDS-PAGE
Form/Format
Lyophilized from sterile PBS, pH 7.4
Sequence Length
1379
Application Notes
The recombinant mouse Met/Fc chimera is a disulfide-linked homodimer of the Met which is a heterodimer composed of the proteolytically cleaved alpha and beta subunits. Each alpha and beta together with the C-terminal Fc tag consists of 1146 amino acids and has a predicted molecular mass of 128 (alpha =32 + Fc tagged beta=96) kDa. The apparent molecular mass of the rm MET/Fc heterodimer thus is approximately 43 kDa and 115-120 kDa respectively in SDS-PAGE under reducing conditions due to glycosylation.
Predicted N Terminal
Glu 25 & Ser 307
Endotoxin
< 1.0 EU per mug of the protein as determined by the LAL method
Preparation and Storage
Samples are stable for up to twelve months from date of receipt at -70 degree C

SDS-PAGE

SDS-PAGE
Related Product Information for c-MET / HGFR recombinant protein
Background: Hepatocyte growth factor receptor (HGFR), also known as c-Met or mesenchymal-epithelial transition factor (MET), is a receptor tyrosine kinase (RTK) that has been shown to be overexpressed and/or mutated in a variety of malignancies. HGFR protein is produced as a single-chain precursor, and HGF is the only known ligand. Normal HGF/HGFR signaling is essential for embryonic development, tissue repair or wound healing, whereas aberrantly active HGFR has been strongly implicated in tumorigenesis, particularly in the development of invasive and metastatic phenotype s. HGFR protein is a multifaceted regulator of growth, motility, and invasion, and is normally expressed by cells of epithelial origin. Preclinical studies suggest that targeting aberrant HGFR signaling could be an attractive therapy in cancer.

Description: A DNA sequence encoding the mouse MET (NP_032617.2) extracellular domain (Met 1-Asn 929) was fused with the Fc region of human IgG1 at the C-terminus.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
153,549 Da
NCBI Official Full Name
hepatocyte growth factor receptor
NCBI Official Synonym Full Names
met proto-oncogene
NCBI Official Symbol
Met
NCBI Official Synonym Symbols
HGF; HGFR; Par4; c-Met; AI838057
NCBI Protein Information
hepatocyte growth factor receptor
UniProt Protein Name
Hepatocyte growth factor receptor
UniProt Gene Name
Met
UniProt Synonym Gene Names
HGF receptor; SF receptor

Uniprot Description

Met: a proto-oncogenic receptor tyrosine kinase with high affinity for hepatocyte growth factor. The primary single chain precursor protein is post-translationally cleaved to produce the 45 kDa alpha- and 145 kDa beta-subunits, which are disulfide linked to form the mature receptor. Ligand-binding induces autophosphorylation at multiple tyrosines, which recruit several downstream signaling components, including Gab1, c-Cbl and PI3 kinase. Activating point mutations cause hereditary papillary renal carcinoma. Mutations also seen in sporadic renal cell carcinoma and childhood hepatocellular carcinoma. Upregulation in carcinomas and sarcomas correlates with metastasis and poor outcome. Some gastric carcinomas harbor a translocation that creates an activated TPR-Met fusion protein. A small molecule inhibitor (PHA-665752) shows an effect in gastric carcinoma xenografts. Inhibitors: SU11274, PHA-665752, mAbs. Two alternatively spliced human isoforms have been reported.

Protein type: EC 2.7.10.1; Kinase, protein; Membrane protein, integral; Met family; Oncoprotein; Protein kinase, TK; Protein kinase, tyrosine (receptor); TK group

Chromosomal Location of Human Ortholog: 6 A2|6 7.83 cM

Cellular Component: basal plasma membrane; cell soma; cell surface; cytoplasm; dendrite; excitatory synapse; extracellular space; membrane; neuron projection; plasma membrane; postsynaptic density; postsynaptic membrane

Molecular Function: beta-catenin binding; hepatocyte growth factor receptor activity; phosphoinositide 3-kinase binding; phospholipase binding; protein complex binding; protein heterodimerization activity; protein kinase activity; protein phosphatase binding; protein-tyrosine kinase activity

Biological Process: activation of MAPK activity; adult behavior; brain development; branching morphogenesis of a tube; cardiac muscle cell development; cardiac muscle contraction; endothelial cell morphogenesis; glucose homeostasis; hepatocyte growth factor receptor signaling pathway; liver development; muscle cell migration; muscle development; myoblast proliferation; myotube differentiation; negative regulation of transcription from RNA polymerase II promoter; neuron migration; placenta development; positive chemotaxis; positive regulation of dendrite morphogenesis; positive regulation of DNA replication; positive regulation of mitosis; positive regulation of peptidyl-serine phosphorylation; positive regulation of transcription from RNA polymerase II promoter; protein amino acid autophosphorylation; regulation of excitatory postsynaptic membrane potential; regulation of interleukin-6 production; regulation of synaptic transmission; skeletal muscle development; sperm motility; synaptic transmission

Research Articles on c-MET / HGFR

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Product Notes

The c-MET / HGFR met (Catalog #AAA2546883) is a Recombinant Protein produced from Human Cells and is intended for research purposes only. The product is available for immediate purchase. The recombinant mouse Met/Fc chimera is a disulfide-linked homodimer of the Met which is a heterodimer composed of the proteolytically cleaved alpha and beta subunits. Each alpha and beta together with the C-terminal Fc tag consists of 1146 amino acids and has a predicted molecular mass of 128 (alpha =32 + Fc tagged beta=96) kDa. The apparent molecular mass of the rm MET/Fc heterodimer thus is approximately 43 kDa and 115-120 kDa respectively in SDS-PAGE under reducing conditions due to glycosylation. Researchers should empirically determine the suitability of the c-MET / HGFR met for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "c-MET / HGFR, Recombinant Protein" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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