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VEGF 165 (AA 27-191) (Active) Protein

Origin: Human Host: HEK-293T Cells Recombinant > 95 % as analyzed by SDS-PAGE. Active
Catalog No. ABIN2018445
  • Target
    VEGF 165
    Protein Type
    Recombinant
    Biological Activity
    Active
    Protein Characteristics
    AA 27-191
    Origin
    • 18
    • 2
    • 1
    Human
    Source
    • 9
    • 7
    • 2
    • 1
    • 1
    • 1
    HEK-293T Cells
    Characteristics
    ED50 <16 ng/mL, measured in a cell proliferation assay using HUVEC cells.
    Purity
    > 95 % as analyzed by SDS-PAGE.
    Endotoxin Level
    < 0.2 EU/μg, determined by LAL method.
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Reconstituted in ddH2O or PBS at 100 μg/mL.
    Buffer
    Lyophilized after extensive dialysis against PBS.
    Storage
    -80 °C
    Storage Comment
    Lyophilized recombinant Human Vascular Endothelial Growth Factor 165 (VEGF-165) remains stable up to 6 months at -80°C from date of receipt. Upon reconstitution, Human Vascular Endothelial Growth Factor 165 (VEGF-165) should be stable up to 1 week at 4°C or up to 2 months at -20°C.
    Expiry Date
    6 months
  • Target
    VEGF 165
    Alternative Name
    Vascular Endothelial Growth Factor 165 (VEGF165)
    Background
    Vascular Endothelial Growth Factor is a potent growth and angiogenic cytokine. It stimulates proliferation and survival of endothelial cells, and promotes angiogenesis and vascular permeability. Expressed in vascularized tissues, VEGF plays a prominent role in normal and pathological angiogenesis. Substantial evidence implicates VEGF in the induction of tumor metastasis and intra-ocular neovascular syndromes. VEGF signals through the three receptors, fms-like tyrosine kinase (flt-1), KDR gene product (the mouse homolog of KDR is the flk-1 gene product) and the flt4 gene product.
    Synonyms: Vascular Endothelial Growth Factor, VPF, Folliculostellate cell-derived growth factor, Glioma-derived endothelial cell mitogen
    Molecular Weight
    20-26 kDa, observed by reducing SDS-PAGE.
    NCBI Accession
    NP_001165097
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