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VEGF-A is a member of the PDGF/VEGF family of growth factors that regulates development, proliferation, and maintenance of the vascular system.1 Alternative splicing of Vegfa pre-mRNA generates two families of variants, pro-angiogenic VEGF-Axxx and anti-angiogenic VEGF-Axxxb isoforms, where xxx indicates the number of amino acids in the mature protein.2,3 VEGF-A exists as a secreted or membrane-bound homodimer composed of an N-terminal signal peptide, which is cleaved in the mature protein, a central VEGF homology domain containing the receptor-binding region, and a variable C-terminal domain containing heparin- or neuropilin-binding sites.4 It is secreted by numerous cell types, including endothelial cells, fibroblasts, smooth muscle cells, platelets, macrophages, and neutrophils, and is induced by inflammation or hypoxia. VEGF-A binds to VEGFR1 and VEGFR2, which are expressed by endothelial cells, to regulate angiogenesis and vascular permeability, as well as cell proliferation, survival, and migration, in an isoform-dependent manner. VEGFA SNPs have been found in patients with a variety of cancers, including breast, prostate, or colorectal cancers.2 Cayman's VEGF-A (C-Term) Rabbit Monoclonal Antibody (RM391) can be used for immunohistochemistry (IHC) and Western blot (WB) applications.
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1. Vascular endothelial growth factor (VEGF) and its receptor (VEGFR) signaling in angiogenesis: A crucial target for anti-
2. Biology and therapeutic implications of VEGF-
3. VEGF-
4. Molecular pharmacology of VEGF-