Product: Angiopoietin 1 Antibody
Catalog: AF5184
Description: Rabbit polyclonal antibody to Angiopoietin 1
Application: WB IHC
Cited expt.: WB
Reactivity: Human, Mouse, Rat
Prediction: Pig, Bovine, Horse, Sheep, Rabbit, Dog, Chicken
Mol.Wt.: 57 kDa; 58kD(Calculated).
Uniprot: Q15389
RRID: AB_2837670

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 100ul $280 In stock
 200ul $350 In stock

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Product Info

Source:
Rabbit
Application:
WB 1:500-1:2000, IHC 1:50-1:200
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

Reactivity:
Human,Mouse,Rat
Prediction:
Pig(100%), Bovine(100%), Horse(100%), Sheep(92%), Rabbit(100%), Dog(83%), Chicken(92%)
Clonality:
Polyclonal
Specificity:
Angiopoietin 1 Antibody detects endogenous levels of total Angiopoietin 1.
RRID:
AB_2837670
Cite Format: Affinity Biosciences Cat# AF5184, RRID:AB_2837670.
Conjugate:
Unconjugated.
Purification:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
Storage:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias:

Fold/Unfold

AGP 1; AGP1; AGPT; ANG 1; ANG; ANG-1; ANG1; Angiopoietin-1; Angiopoietin1; ANGP1_HUMAN; ANGPT 1; Angpt1; KIAA0003; OTTHUMP00000227592; OTTHUMP00000227599; OTTHUMP00000227600;

Immunogens

Immunogen:

A synthesized peptide derived from human Angiopoietin 1, corresponding to a region within the internal amino acids.

Uniprot:
Gene(ID):
Description:
Binds and activates TEK/TIE2 receptor by inducing its dimerization and tyrosine phosphorylation. Plays an important role in the regulation of angiogenesis, endothelial cell survival, proliferation, migration, adhesion and cell spreading, reorganization of the actin cytoskeleton, but also maintenance of vascular quiescence
Sequence:
MTVFLSFAFLAAILTHIGCSNQRRSPENSGRRYNRIQHGQCAYTFILPEHDGNCRESTTDQYNTNALQRDAPHVEPDFSSQKLQHLEHVMENYTQWLQKLENYIVENMKSEMAQIQQNAVQNHTATMLEIGTSLLSQTAEQTRKLTDVETQVLNQTSRLEIQLLENSLSTYKLEKQLLQQTNEILKIHEKNSLLEHKILEMEGKHKEELDTLKEEKENLQGLVTRQTYIIQELEKQLNRATTNNSVLQKQQLELMDTVHNLVNLCTKEGVLLKGGKREEEKPFRDCADVYQAGFNKSGIYTIYINNMPEPKKVFCNMDVNGGGWTVIQHREDGSLDFQRGWKEYKMGFGNPSGEYWLGNEFIFAITSQRQYMLRIELMDWEGNRAYSQYDRFHIGNEKQNYRLYLKGHTGTAGKQSSLILHGADFSTKDADNDNCMCKCALMLTGGWWFDACGPSNLNGMFYTAGQNHGKLNGIKWHYFKGPSYSLRSTTMMIRPLDF

Predictions

Predictions:

Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Rabbit
100
Sheep
92
Chicken
92
Dog
83
Xenopus
75
Zebrafish
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

Research Backgrounds

Function:

Binds and activates TEK/TIE2 receptor by inducing its dimerization and tyrosine phosphorylation. Plays an important role in the regulation of angiogenesis, endothelial cell survival, proliferation, migration, adhesion and cell spreading, reorganization of the actin cytoskeleton, but also maintenance of vascular quiescence. Required for normal angiogenesis and heart development during embryogenesis. After birth, activates or inhibits angiogenesis, depending on the context. Inhibits angiogenesis and promotes vascular stability in quiescent vessels, where endothelial cells have tight contacts. In quiescent vessels, ANGPT1 oligomers recruit TEK to cell-cell contacts, forming complexes with TEK molecules from adjoining cells, and this leads to preferential activation of phosphatidylinositol 3-kinase and the AKT1 signaling cascades. In migrating endothelial cells that lack cell-cell adhesions, ANGT1 recruits TEK to contacts with the extracellular matrix, leading to the formation of focal adhesion complexes, activation of PTK2/FAK and of the downstream kinases MAPK1/ERK2 and MAPK3/ERK1, and ultimately to the stimulation of sprouting angiogenesis. Mediates blood vessel maturation/stability. Implicated in endothelial developmental processes later and distinct from that of VEGF. Appears to play a crucial role in mediating reciprocal interactions between the endothelium and surrounding matrix and mesenchyme.

PTMs:

Glycosylated.

Subcellular Location:

Secreted.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location

Research Fields

· Environmental Information Processing > Signal transduction > MAPK signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Ras signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Rap1 signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > HIF-1 signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > PI3K-Akt signaling pathway.   (View pathway)

· Human Diseases > Immune diseases > Rheumatoid arthritis.

References

1). Analysis of Expression of the ANG1, CaSR and FAK Proteins in Uterine Fibroids. International journal of molecular sciences, 2024 (PubMed: 39000274) [IF=5.6]

2). Adhesive, injectable, and ROS-responsive hybrid polyvinyl alcohol (PVA) hydrogel co-delivers metformin and fibroblast growth factor 21 (FGF21) for enhanced diabetic wound repair. Frontiers in bioengineering and biotechnology, 2022 (PubMed: 36118565) [IF=4.3]

Application: WB    Species: Rat    Sample: wound tissues

FIGURE 7. (A) Immunofluorescence staining of α-SMA (green) of wound tissues on days 8 and 14 (scale bars: 50 μm). (B) Quantified data of vessels number per field. (C) Western blot analysis of Ang-1 expression. (D) Quantitative analysis of Ang-1 protein expression based on Western blot. *p < 0.05; **p < 0.01 compared with control, n = 3.

3). hUCMSCs restore ovarian function via angiopoietin 1/2 rebalance in POI rats. Journal of ovarian research, 2025 (PubMed: 41254793) [IF=4.0]

Application: WB    Species: human    Sample:

Fig. 4 hUCMSCs restore ovarian angiogenesis by rebalancing Angpt1/Angpt2 in POI. A Immunofluorescence detection of Angpt1, Angpt2 and CD31 expression in the ovaries from control, POI and POI + hUCMSCs group. DAPI repainted nucleus are blue, Angpt1 and Angpt2 positive are green, CD31 positive is red. scale bar is 60 μm. B Western blot of CD31, Angpt1, Angpt2, and GAPDH in ovarian tissues across groups. C-E Quantitative analysis of Angpt1, Angpt2 and CD31(normalized to GAPDH). F. The ratio of Angpt1/Angpt2 at protein level. G-I Quantification of Angpt1, Angpt2 and mRNA expression ratio. J. Correlation between Angpt1/Angpt2 protein ratio and CD31 at protein level. Data were shown as mean ± SD of at least three independent experiments. *: P

Application: IF/ICC    Species: human    Sample:

Fig. 4 hUCMSCs restore ovarian angiogenesis by rebalancing Angpt1/Angpt2 in POI. A Immunofluorescence detection of Angpt1, Angpt2 and CD31 expression in the ovaries from control, POI and POI + hUCMSCs group. DAPI repainted nucleus are blue, Angpt1 and Angpt2 positive are green, CD31 positive is red. scale bar is 60 μm. B Western blot of CD31, Angpt1, Angpt2, and GAPDH in ovarian tissues across groups. C-E Quantitative analysis of Angpt1, Angpt2 and CD31(normalized to GAPDH). F. The ratio of Angpt1/Angpt2 at protein level. G-I Quantification of Angpt1, Angpt2 and mRNA expression ratio. J. Correlation between Angpt1/Angpt2 protein ratio and CD31 at protein level. Data were shown as mean ± SD of at least three independent experiments.

4). Bone marrow-derived mesenchymal stem cells transplantation attenuates renal fibrosis following acute kidney injury by repairing the peritubular capillaries. Experimental Cell Research, 2022 (PubMed: 34921827) [IF=3.3]

5). Danshen/Huanglian-loaded gelatin/Bletilla striata gum dressings accelerate wound healing in anal fistula by promoting angiogenesis through TGF-β/Smad pathway activation. Journal of molecular histology, 2026 (PubMed: 41528408) [IF=2.9]

6). Daidzein alleviates osteoporosis by promoting osteogenesis and angiogenesis coupling. PeerJ, 2023 (PubMed: 37868048) [IF=2.3]

Application: WB    Species: Rat    Sample: BMECs

Figure 3: Daidzein improves migration and proliferation of BMECs. (A) BMECs were cultured and treated with different dose of daidzein (0, 10, 20 µM). Scratch wound healing assay was performed to observe the effect of daidzein on the migration of BMECs. Scale bar, 100 µm. (B) Quantitative analysis of wound healing rate. (C) Representative images of immunofluorescence staining for Ki67 (green) in BMECs treated with different dose of daidzein (0, 10 µM). Nuclei were stained with DAPI (blue). White arrows indicate Ki67+ cells. Scale bar, 100 µm. (D) Quantification of the percentage of Ki67+ nuclei among the total nuclei. (E, F) RNA was isolated from BMECs in the control and daidzein groups, and the mRNA expression of Angpt-1 and Vegf was detected with qRT-PCR. (G) BMECs were cultured and treated with different dose of daidzein, protein was harvested at indicated time points, western blotting was performed to detect the expression and ANGPT-1 phospho-VEGFR and GAPDH was used as reference proteins for data normalization. (H) ANGPT-1 and phosphorylation levels of VEGFR were quantified and normalized to total VEGFR. Data were presented as mean ± SE. *p < 0.05 and **p < 0.01 as determined by One way ANOVA or two-tailed unpaired t-test.

7). Experimental study of slow-released Angiogenin by silicon micro-needle in improving blood support to multiple-territory perforator flaps in rats. Cellular and molecular biology (Noisy-le-Grand, France), 2024 (PubMed: 38836686) [IF=1.5]

8). [Dose and timing of normal saline resuscitation on endothelial glycocalyx in early septic shock]. , 2018 (PubMed: 30045788)

9). Immunohistochemical Expression of the ANGPT1, Casr and PTK2 Proteins in Uterine Fibroids. , 2023

10). Xiaoyukang Jiaonang Promotes the Degradation of Hypoxia-Inducible Factor 1 α and Antiangiogenesis and Anti-Inflammation in Chronic Subdural Hematoma Rat Model. Evidence-based complementary and alternative medicine : eCAM, 2020 (PubMed: 32328124)

Application: WB    Species: Rat    Sample:

Figure 1 (e) In the XYK group, HIF-1α and VEGF decreased, E3 ubiquitin-protein ligase parkin and 26S proteasome protein increased, and the Ang-1/Ang-2 ratio increased in the hematoma. Western blots analysis of HIF-1α, E3 ubiquitin-protein ligase parkin, and 26S proteasome protein in hematoma (A-D). Western blots analysis of VEGF, Ang-1, and Ang-2 (E-I).  ∗P < 0.05 and  ∗∗P < 0.01. Ang, angiopoietins; CSDH, chronic subdural hematoma HIF, hypoxia-inducible factor; VEGF, vascular endothelial growth factor; XYK, Xiaoyukang Jiaonang.

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