Description : |
This gene is a member of the PDGF/VEGF growth factor family. It encodes a heparin-binding protein, which exists as a disulfide-linked homodimer. This growth factor induces proliferation and migration of vascular endothelial cells, and is essential for both physiological and pathological angiogenesis. Disruption of this gene in mice resulted in abnormal embryonic blood vessel formation. This gene is upregulated in many known tumors and its expression is correlated with tumor stage and progression. Elevated levels of this protein are found in patients with POEMS syndrome, also known as Crow-Fukase syndrome. Allelic variants of this gene have been associated with microvascular complications of diabetes 1 (MVCD1) and atherosclerosis. Alternatively spliced transcript variants encoding different isoforms have been described. |
Source : |
CHO-K1 |
Species : |
Human |
Form : |
Lyophilized powder |
Endotoxin : |
<20 EU/mg |
Bio-activity : |
ED50 of 1-4ng/ml (dose-dependent stimulation of human umbilical vein endothelial cell proliferation) |
Purity : |
>95.0% by high performance liquid chromatography (SEC-HPLC) and SDS-PAGE. |
Storage Buffer : |
10mM Phosphate-Buffered Saline (pH 7.2) |
Storage : |
Stable storage at 4℃ for 7-10 days; for long-term storage, please store at -20℃ after dispensing. |
Sterility : |
Sterility |
Instructions : |
It is recommended that lyophilized GMP rhVEGFA be dissolved in water for injection or sterilized ultrapure water at a concentration of not less than 100 μg/ml, pending further dilution to working concentration. |