Recombinant Anti-c-MET/HGFR Antibody, Rabbit Monoclonal sinobiological 50622-R001

$171.00
In stock
SKU
50622-R001
Catalog No.SizePrice (USD)
50622-R001-5050 µL$177.58
50622-R001-100100 µL$340.51

General Information

Product nameRecombinant Anti-c-MET/HGFR Antibody, Rabbit Monoclonal
Validated applicationsELISA (FAQ Protocol)
Species reactivityReacts with: Mouse
SpecificityMouse c-MET/HGFR
ImmunogenRecombinant Mouse c-Met/Met/HGFR Protein (Catalog#50622-M08H)
PreparationThis antibody was obtained from a rabbit immunized with purified, recombinant Mouse c-Met/Met/HGFR (rM c-Met/Met/HGFR; Catalog#50622-M08H;EDL13881.1; Met1-Asn929).
SourceMonoclonal Rabbit IgG Clone #001
PurificationProtein A
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-c-Met Antibody; Anti-HGF Antibody; Anti-HGFR Antibody; Anti-Met Antibody; Anti-Par4 Antibody

Background Information

Full NameMET proto-oncogene, receptor tyrosine kinase
DescriptionHepatocyte growth factor receptor (HGFR), also known as c-Met or mesenchymal-epithelial transition factor (MET), is a receptor tyrosine kinase (RTK) that is 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 phenotypes. 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.
Research Areas
  • Cancer Drug Targets
  • Receptor Tyrosine Kinases (RTKs)
Tags
  • Cancer Immunotherapy
  • Immune Checkpoint
  • Immunotherapy
  • Targeted Therapy
References
  1. McGill GG, et al. (2006) c-Met expression is regulated by Mitf in the melanocyte lineage. J Biol Chem. 281(15): 10365-73.
  2. Garcia S, et al. (2007) c-Met overexpression in inflammatory breast carcinomas: automated quantification on tissue microarrays. British journal of cancer. 96(2): 329-35.
  3. Socoteanu MP, et al. (2008) c-Met targeted therapy of cholangiocarcinoma. World J Gastroenterol. 14(19): 2990-4.
  4. Kong DS, et al. (2009) Prognostic significance of c-Met expression in glioblastomas. Cancer. 115(1): 140-8.

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