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Read our guarantee »Products:Cardiovascular >> Angiogenesis >> Growth Factors >> Angiopoietin
Anti-Angiopoietin 2 antibody
Angiopoietin 2 抗体 (4件) 一覧
Rabbit polyclonal to Angiopoietin 2
This antibody is specific for mouse Angiopoietin 2 (mAng-2), and shows a band at 75kD.
ICC/IF, IHC-Fr, WBmore details
Reacts with
Mouse, Human
Synthetic peptide: CNNFRKSVDSTGRRQYQVQNGP, corresponding to amino acids 21-40 of Mouse Angiopoietin 2. (Peptide available as ab9077).
CNNFRKSVDS TGRRQYQVQN GP
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
0.02 K Phosphate, 0.15M NaCl, 0.1% Sodium Azide, pH7.2
Whole antiserum
Polyclonal
IgG
Cardiovascular >> Angiogenesis >> Growth Factors >> Angiopoietin
Our Abpromise guarantee covers the use of ab8452 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: 1/200
IHC-Fr: Use at an assay dependent dilution. (PubMed: 19553662Use at an assay dependent dilution (PMID 19553662).)
WB: 1/500(There is reaction with serum in the cell supernatants, which results in strong background and makes it difficult to see the angiopoietins in cell supernatants. However when precipitated (using soluble Tie2) the signals are very good and strong.)
Can induce tyrosine phosphorylation of TIE2. Binds to TIE2 receptor and counteracts blood vessel maturation/stability mediated by angiopoietin-1. Its function may be context-dependent. In the absence of angiogenic inducers, such as VEGF, ANG2-mediated loosening of cell-matrix contacts may induce endothelial cell apoptosis with consequent vascular regression. In concert with VEGF, it may facilitate endothelial cell migration and proliferation, thus serving as a permissive angiogenic signal.
Contains 1 fibrinogen C-terminal domain.
The Fibrinogen C-terminal domain mediates interaction with the TEK/TIE2 receptor.
Secreted.
Target information above from: UniProt accessionO15123
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Angiopoietin 2 antibody (ab8452)

Supernatants of mouse angiopoietin-expressing endothelial cells. Soluble Tie 2 was used to precipitate the angiopoietins to reduce background.
Lane 1 - mock
Lane 2 - mouse angiopoietin-2 (clone 2-9) expressing cells
Lane 3 - mouse angiopoietin-1 (clone 1-15) expressing cells
Lane 4 - mouse angiopoietin-1 (clone 1-8) expressing cells
Lane 5 - wt
Marion Scharpfenecker 2002
Immunocytochemistry/ Immunofluorescence - Angiopoietin 2 antibody (ab8452)

ICC/IF image of ab8452 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8452, 1/200 dilution) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab8452? Please let us know so that we can cite the reference in this datasheet
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Supernatants of mouse angiopoietin-expressing endothelial cells. Soluble Tie 2 was used to precipitate the angiopoietins to reduce background.
Lane 1 - mock
Lane 2 - mouse angiopoietin-2 (clone 2-9) expressing cells
Lane 3 - mouse angiopoietin-1 (clone 1-15) expressing cells
Lane 4 - mouse angiopoietin-1 (clone 1-8) expressing cells
Lane 5 - wt
Marion Scharpfenecker 2002

ICC/IF image of ab8452 stained PC12 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8452, 1/200 dilution) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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