Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Immunohistochemistry [1]
- Flow cytometry [2]
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Validation data
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- Product number
- PA5-23612 - Provider product page

- Provider
- Invitrogen Antibodies
- Product name
- Angiopoietin 2 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 400 μL
- Concentration
- 2.0 mg/mL
- Storage
- Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Submitted references Mitochondrial complex III is necessary for endothelial cell proliferation during angiogenesis.
Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS
Nature metabolism 2019 Jan;1(1):158-171
Nature metabolism 2019 Jan;1(1):158-171
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- Immunohistochemistry analysis of Angiopoietin 2 in formalin fixed and paraffin embedded human uterus tissue. Samples were incubated with Angiopoietin 2 polyclonal antibody (Product # PA5-23612) followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of this antibody for immunohistochemistry. Clinical relevance has not been evaluated.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- Flow cytometry analysis of A549 cells using an ANGPT2 polyclonal antibody (Product # PA5-23612) (right) compared to a negative control cell (left) at a dilution of 1:10-50, followed by a FITC-conjugated goat anti-rabbit antibody
- Submitted by
- Invitrogen Antibodies (provider)
- Main image

- Experimental details
- Flow cytometry of (overlay histogram) of Angiopoietin 2 in A549 cells (green line). Samples were incubated with Angiopoietin 2 polyclonal antibody (Product # PA5-23612) using a dilution of 1:25 dilution for 60 min at 37°C followed by Goat-Anti-Rabbit IgG, DyLight® 488 Conjugated Highly Cross-Adsorbed at 1:200 dilution for 40 min at 37°C. The cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with 90% methanol for 10 min. The cells were then incubated in 2% bovine serum albumin to block non-specific protein-protein interactions followed by the primary antibody. Isotype control antibody (blue line) was rabbit IgG (1 μg/1x10^6 cells) used under the same conditions. Acquisition of >10, 000 events was performed.