hif 1 α antibody Search Results


96
Proteintech membranes
Membranes, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Santa Cruz Biotechnology anti hif 1α
Anti Hif 1α, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proteintech hif 1α
Hif 1α, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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hif 1α - by Bioz Stars, 2026-03
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90
ImmunoWay Biotechnology Company hif-1α yt2133 antibody
Hif 1α Yt2133 Antibody, supplied by ImmunoWay Biotechnology Company, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson anti-hif1a
Anti Hif1a, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cayman Chemical hif-1α (1:500; catlog no. 10006421;
Hif 1α (1:500; Catlog No. 10006421;, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hif-1α (1:500; catlog no. 10006421;/product/Cayman Chemical
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GeneTex anti-hif2-a
Anti Hif2 A, supplied by GeneTex, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Servicebio Inc primary antibodies against hif-1α gb13031-1
a Biodistribution of DR-CoMo-LDH-PEG in mice by monitoring the Co concentration at various time points post-injection. Data are presented as mean values ± s.d. ( n = 3). Statistical analysis was performed via one-way ANOVA. *p < 0.05, **p < 0.01, ***p < 0.001. b Tumor growth curves of mice after various treatments. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. c Representative photographs of mice with treatments at various time points and d corresponding average weight of tumors taken on Day 16. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. e Body weight change of 4T1 tumor-bearing mice after different treatments. Data are presented as mean values ± s.d. ( n = 6). f <t>HIF-1α,</t> g DHE, and h H&E, Ki-67, TUNEL and CD31 staining assay of tumor slices from various groups of mice after 16 days of treatment: 1) PBS, 2) 1567 nm laser (0.5 W cm −2 for 6 min), 3) DR-CoMo-LDH-PEG, 4) DR-CoMo-LDH-PEG + 1567 nm laser. Each experiment was repeated three times with similar results. Source data are provided as a Source Data file.
Primary Antibodies Against Hif 1α Gb13031 1, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies against hif-1α gb13031-1/product/Servicebio Inc
Average 90 stars, based on 1 article reviews
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Absolute Biotech Inc anti-hif-1α monoclonal antibody ls-b145/10218
a Biodistribution of DR-CoMo-LDH-PEG in mice by monitoring the Co concentration at various time points post-injection. Data are presented as mean values ± s.d. ( n = 3). Statistical analysis was performed via one-way ANOVA. *p < 0.05, **p < 0.01, ***p < 0.001. b Tumor growth curves of mice after various treatments. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. c Representative photographs of mice with treatments at various time points and d corresponding average weight of tumors taken on Day 16. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. e Body weight change of 4T1 tumor-bearing mice after different treatments. Data are presented as mean values ± s.d. ( n = 6). f <t>HIF-1α,</t> g DHE, and h H&E, Ki-67, TUNEL and CD31 staining assay of tumor slices from various groups of mice after 16 days of treatment: 1) PBS, 2) 1567 nm laser (0.5 W cm −2 for 6 min), 3) DR-CoMo-LDH-PEG, 4) DR-CoMo-LDH-PEG + 1567 nm laser. Each experiment was repeated three times with similar results. Source data are provided as a Source Data file.
Anti Hif 1α Monoclonal Antibody Ls B145/10218, supplied by Absolute Biotech Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Upstate Biotechnology Inc antibodies against human hif-1
a Biodistribution of DR-CoMo-LDH-PEG in mice by monitoring the Co concentration at various time points post-injection. Data are presented as mean values ± s.d. ( n = 3). Statistical analysis was performed via one-way ANOVA. *p < 0.05, **p < 0.01, ***p < 0.001. b Tumor growth curves of mice after various treatments. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. c Representative photographs of mice with treatments at various time points and d corresponding average weight of tumors taken on Day 16. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. e Body weight change of 4T1 tumor-bearing mice after different treatments. Data are presented as mean values ± s.d. ( n = 6). f <t>HIF-1α,</t> g DHE, and h H&E, Ki-67, TUNEL and CD31 staining assay of tumor slices from various groups of mice after 16 days of treatment: 1) PBS, 2) 1567 nm laser (0.5 W cm −2 for 6 min), 3) DR-CoMo-LDH-PEG, 4) DR-CoMo-LDH-PEG + 1567 nm laser. Each experiment was repeated three times with similar results. Source data are provided as a Source Data file.
Antibodies Against Human Hif 1, supplied by Upstate Biotechnology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antibodies against human hif-1/product/Upstate Biotechnology Inc
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90
ZenBio hif-1α antibody
Diabetes impedes neovascularization level in spinal cord of SCI rat. (A and B) Representative western blotting results and quantitative analysis of <t>HIF-1α,</t> ANG1 and VEGF in spinal cord at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.
Hif 1α Antibody, supplied by ZenBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hif-1α antibody/product/ZenBio
Average 90 stars, based on 1 article reviews
hif-1α antibody - by Bioz Stars, 2026-03
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90
Beyotime hif1α
Diabetes impedes neovascularization level in spinal cord of SCI rat. (A and B) Representative western blotting results and quantitative analysis of <t>HIF-1α,</t> ANG1 and VEGF in spinal cord at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.
Hif1α, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hif1α/product/Beyotime
Average 90 stars, based on 1 article reviews
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Image Search Results


a Biodistribution of DR-CoMo-LDH-PEG in mice by monitoring the Co concentration at various time points post-injection. Data are presented as mean values ± s.d. ( n = 3). Statistical analysis was performed via one-way ANOVA. *p < 0.05, **p < 0.01, ***p < 0.001. b Tumor growth curves of mice after various treatments. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. c Representative photographs of mice with treatments at various time points and d corresponding average weight of tumors taken on Day 16. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. e Body weight change of 4T1 tumor-bearing mice after different treatments. Data are presented as mean values ± s.d. ( n = 6). f HIF-1α, g DHE, and h H&E, Ki-67, TUNEL and CD31 staining assay of tumor slices from various groups of mice after 16 days of treatment: 1) PBS, 2) 1567 nm laser (0.5 W cm −2 for 6 min), 3) DR-CoMo-LDH-PEG, 4) DR-CoMo-LDH-PEG + 1567 nm laser. Each experiment was repeated three times with similar results. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Defect engineering of layered double hydroxide nanosheets as inorganic photosensitizers for NIR-III photodynamic cancer therapy

doi: 10.1038/s41467-022-31106-9

Figure Lengend Snippet: a Biodistribution of DR-CoMo-LDH-PEG in mice by monitoring the Co concentration at various time points post-injection. Data are presented as mean values ± s.d. ( n = 3). Statistical analysis was performed via one-way ANOVA. *p < 0.05, **p < 0.01, ***p < 0.001. b Tumor growth curves of mice after various treatments. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. c Representative photographs of mice with treatments at various time points and d corresponding average weight of tumors taken on Day 16. Data are presented as mean values ± s.d. ( n = 6). Statistical analysis was performed via one-way ANOVA. ***p < 0.001. e Body weight change of 4T1 tumor-bearing mice after different treatments. Data are presented as mean values ± s.d. ( n = 6). f HIF-1α, g DHE, and h H&E, Ki-67, TUNEL and CD31 staining assay of tumor slices from various groups of mice after 16 days of treatment: 1) PBS, 2) 1567 nm laser (0.5 W cm −2 for 6 min), 3) DR-CoMo-LDH-PEG, 4) DR-CoMo-LDH-PEG + 1567 nm laser. Each experiment was repeated three times with similar results. Source data are provided as a Source Data file.

Article Snippet: The tumor slices were stained with primary antibodies (against HIF-1α (GB13031-1, Servicebio, China, 1:200 dilution)) at 4 °C overnight, followed by phalloidin at 25 °C for 1 h. Images were captured via CLSM.

Techniques: Concentration Assay, Injection, TUNEL Assay, Staining

Diabetes impedes neovascularization level in spinal cord of SCI rat. (A and B) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in spinal cord at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.

Journal: International Journal of Biological Sciences

Article Title: Over-activation of TRPM2 ion channel accelerates blood-spinal cord barrier destruction in diabetes combined with spinal cord injury rat

doi: 10.7150/ijbs.80672

Figure Lengend Snippet: Diabetes impedes neovascularization level in spinal cord of SCI rat. (A and B) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in spinal cord at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.

Article Snippet: Then, the membranes were blocked with 5% skimmed milk in TBST for 2 h at room temperature, and incubated with the following primary antibodies at 4°C overnight: TRPM2 (1:1000, NB500-242), p-CaMKII (1:1000, sc-32289), CaMKII (1:1000, sc-5306), eNOS (1:1000, sc-376751), NOX2 (1:1000, ab129068), HIF-1α (1:1000, ZEN BIO, 340462), ANG1 (1:5000, ab183701), VEGF (1:1000, sc-7269), Cleaved(C)-caspase3 (1:1000, 9664S), β-catenin (1:1000, ab32572), ZO-1 (1:1000, AF5145), Claudin-5 (1:1000, AF5216), occluding (1:1000, DF7504), P120 (1:1000, AF4684).

Techniques: Western Blot, Staining, Tube Formation Assay

TRPM2 inhibition improves angiogenesis level under diabetes combined with SCI condition. (A and B) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in spinal cord of rat at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200 μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.

Journal: International Journal of Biological Sciences

Article Title: Over-activation of TRPM2 ion channel accelerates blood-spinal cord barrier destruction in diabetes combined with spinal cord injury rat

doi: 10.7150/ijbs.80672

Figure Lengend Snippet: TRPM2 inhibition improves angiogenesis level under diabetes combined with SCI condition. (A and B) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in spinal cord of rat at 3 days after SCI. (C and D) Representative western blotting results and quantitative analysis of HIF-1α, ANG1 and VEGF in HUVECs. (E) Co-staining of HIF-1α (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (F) Co-staining of ANG1 (green) and CD31 (red) in spinal cord at 3 days after SCI, Scale bar = 10 μm. (G) The tube formation ability of HUVECs, Scale bar = 200 μm. (H) Quantification of tube length from tube formation assay. n≥3, *P<0.05, **P<0.01, ***P<0.001.

Article Snippet: Then, the membranes were blocked with 5% skimmed milk in TBST for 2 h at room temperature, and incubated with the following primary antibodies at 4°C overnight: TRPM2 (1:1000, NB500-242), p-CaMKII (1:1000, sc-32289), CaMKII (1:1000, sc-5306), eNOS (1:1000, sc-376751), NOX2 (1:1000, ab129068), HIF-1α (1:1000, ZEN BIO, 340462), ANG1 (1:5000, ab183701), VEGF (1:1000, sc-7269), Cleaved(C)-caspase3 (1:1000, 9664S), β-catenin (1:1000, ab32572), ZO-1 (1:1000, AF5145), Claudin-5 (1:1000, AF5216), occluding (1:1000, DF7504), P120 (1:1000, AF4684).

Techniques: Inhibition, Western Blot, Staining, Tube Formation Assay