Description:
The onset of angiogenesis is believed to be an early event in
tumorigenesis and may facilitate tumor progression and metastasis.
Several growth factors with angiogenic activity have been described.
These include fibroblast growth factors (FGFs), platelet derived
growth factor (PDGF) and vascular endothelial growth factor (VEGF).
VEGF is a dimeric glycoprotein with structural homology to PDGF.
Several variants of VEGF have been described that arise by
alternative mRNA splicing. It has been speculated that VEGF may
function as a tumor angiogenesis factor
in vivo because the
expression pattern of VEGF is consistent with a role in embryonic
angiogenesis. VEGF mRNA is formed in some primary tumors, VEGF is
produced by tumor cell lines
in vitro and VEGF mitogenic activity appears to be restricted to
endothelial cells. A member of the PDGF receptor family, Flt, has
been identified as a high-affinity receptor for VEGF.
Primary Antibody
Name: VEGF (A-20-G) Antibody |
Clone: Goat polyclonal |
Supplier: Santa Cruz Biotechnology |
Catalog Number: sc-152-G |
Dilution: 1:1000 using IHC-TekTM Antibody Diluent (Cat# IW-1000 or IW-1001) to reduce background and unspecific staining and serum blocking step is NOT needed. |
Incubation Time/Temp: 60 min/room temperature |
Device: IHC-TekTM Epitope Retrieval Steamer Set (Cat# IW-1102) |
Buffer/pH value: IHC-TekTM Epitope Retrieval Solution (Cat# IW-1100) |
Heat/Cool Temperature: 95-100 ºC/room temperature |
Heat/Cool Time: 20 minutes/20 minutes |
Standard Method: ABC Method or LSAB Method |
Enhanced Method: Polymeric Methods |
Reagent: DAB |
Incubation Time/Temperature: 1-3 minutes/room temperature |
Reagent: Mayer's Hematoxylin |
Staining Time: 30 seconds |
Staining Pattern: Membrane |
Images: Search image |
Species Reactivity: Human, mouse, rat |
Fixation: Formalin fixed paraffin sections |
Positive Control: Islets of langerhans in pancreas |
Negative Control: Omit primary antibody, isotype control, absorption control |
Blocking: 2-5% normal serum to reduce unspecific background staining; 0.5-3% H2O2 to block endogenous peroxidase activity; avidin/biotin to block endogenous biotin activity if necessary |
References: