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mouse anti vascular endothelial growth factor vegf  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology mouse anti vascular endothelial growth factor vegf
    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes <t>(VEGF,</t> FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).
    Mouse Anti Vascular Endothelial Growth Factor Vegf, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 3169 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+vascular+endothelial+growth+factor/VEGF/pmc12274771-141-46-54
    Average 96 stars, based on 3169 article reviews
    mouse anti vascular endothelial growth factor vegf - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Fabrication of Piezo1 protein encapsulated pressure-sensitive multifunctional hydrogel in modulating cellular response and wound healing in pressure ulcer conditions"

    Article Title: Fabrication of Piezo1 protein encapsulated pressure-sensitive multifunctional hydrogel in modulating cellular response and wound healing in pressure ulcer conditions

    Journal: Regenerative Therapy

    doi: 10.1016/j.reth.2025.06.014

    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes (VEGF, FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).
    Figure Legend Snippet: Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes (VEGF, FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).

    Techniques Used: Gene Expression, Tube Formation Assay



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    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes <t>(VEGF,</t> FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).
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    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes <t>(VEGF,</t> FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).
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    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes <t>(VEGF,</t> FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).
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    BSP upregulated the expression of <t>VEGF</t> and eNOS protein (A) Western blot was used to detect the expression of VEGF and eNOS protein. (B, C) Statistical chart of protein quantitative analysis. Compared with the control group, ***p < 0.001, ****p < 0.0001, compared with the BSP-M group, # p < 0.05, ### p < 0.001, #### p < 0.0001.
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    BSP upregulated the expression of <t>VEGF</t> and eNOS protein (A) Western blot was used to detect the expression of VEGF and eNOS protein. (B, C) Statistical chart of protein quantitative analysis. Compared with the control group, ***p < 0.001, ****p < 0.0001, compared with the BSP-M group, # p < 0.05, ### p < 0.001, #### p < 0.0001.
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    BSP upregulated the expression of <t>VEGF</t> and eNOS protein (A) Western blot was used to detect the expression of VEGF and eNOS protein. (B, C) Statistical chart of protein quantitative analysis. Compared with the control group, ***p < 0.001, ****p < 0.0001, compared with the BSP-M group, # p < 0.05, ### p < 0.001, #### p < 0.0001.
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    Image Search Results


    Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes (VEGF, FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).

    Journal: Regenerative Therapy

    Article Title: Fabrication of Piezo1 protein encapsulated pressure-sensitive multifunctional hydrogel in modulating cellular response and wound healing in pressure ulcer conditions

    doi: 10.1016/j.reth.2025.06.014

    Figure Lengend Snippet: Determination of the angiogenic potential and gene expression of NHI 3T3 and HUVEC cell lines. (A–C) Denotes the number of nodes and segments of 3T3 cell lines and the representative images for tube formation assay. (D–F) Indicates the tube formation changes of HUVEC when treated with PP-MHs. (G & H) Represents the relative mRNA expressions of angiogenic genes (VEGF, FGE2, ADAM19, MM9) in NHI 3T3 and HUVEC cell lines. The data in each bar represents the mean ± SD of three independent samples. They were statistically significant, as indicated by the symbols ∗∗ for ( p < 0.01 ), and ∗∗∗ for ( p < 0.001 ).

    Article Snippet: The membranes were incubated overnight at 4 °C following a blocking procedure with 5 % non-fat milk powder and subsequent treatment with rabbit anti-neutrophil elastase (29 kDa), rabbit anti-precursor transforming growth factor (TGF)-β 1/2/3 antibody, rabbit anti-matrix metalloproteinase (MMP)-12, goat anti-monocyte chemoattractant protein (MCP)-1 antibody, and mouse anti-vascular endothelial growth factor (VEGF) obtained from Santa Cruz Biotechnology.

    Techniques: Gene Expression, Tube Formation Assay

    BSP upregulated the expression of VEGF and eNOS protein (A) Western blot was used to detect the expression of VEGF and eNOS protein. (B, C) Statistical chart of protein quantitative analysis. Compared with the control group, ***p < 0.001, ****p < 0.0001, compared with the BSP-M group, # p < 0.05, ### p < 0.001, #### p < 0.0001.

    Journal: Frontiers in Pharmacology

    Article Title: Bletilla striata polysaccharide induces autophagy through PI3K/AKT signaling pathway to promote the survival of cross-boundary flap in rats

    doi: 10.3389/fphar.2025.1544932

    Figure Lengend Snippet: BSP upregulated the expression of VEGF and eNOS protein (A) Western blot was used to detect the expression of VEGF and eNOS protein. (B, C) Statistical chart of protein quantitative analysis. Compared with the control group, ***p < 0.001, ****p < 0.0001, compared with the BSP-M group, # p < 0.05, ### p < 0.001, #### p < 0.0001.

    Article Snippet: Mouse anti-vascular endothelial growth factor (VEGF), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), PI3K, vascular endothelial cadherin (CDH5), rabbit anti- endothelial nitric oxide synthase (eNOS), AKT, vacuolar protein sorting 34 (VPS34), matrix metalloproteinase 9 (MMP9), microtubule-associated protein light chain 3 (LC3) antibody, HRP goat anti-mouse secondary antibody, HRP goat anti-rabbit secondary antibody (Proteintech Group, Inc.).

    Techniques: Expressing, Western Blot, Control

    The inhibition of autophagy reverse the effect of BSP on blood vessels (A, B) Western blot was used to detecte the expression of VEGF,CDH5,MMP9 and eNOS protein. (C–F) Statistical chart of protein quantitative analysis. Compared with BSP-M group, **p < 0.01, ***p < 0.001, ****p < 0.0001, n = 6.

    Journal: Frontiers in Pharmacology

    Article Title: Bletilla striata polysaccharide induces autophagy through PI3K/AKT signaling pathway to promote the survival of cross-boundary flap in rats

    doi: 10.3389/fphar.2025.1544932

    Figure Lengend Snippet: The inhibition of autophagy reverse the effect of BSP on blood vessels (A, B) Western blot was used to detecte the expression of VEGF,CDH5,MMP9 and eNOS protein. (C–F) Statistical chart of protein quantitative analysis. Compared with BSP-M group, **p < 0.01, ***p < 0.001, ****p < 0.0001, n = 6.

    Article Snippet: Mouse anti-vascular endothelial growth factor (VEGF), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), PI3K, vascular endothelial cadherin (CDH5), rabbit anti- endothelial nitric oxide synthase (eNOS), AKT, vacuolar protein sorting 34 (VPS34), matrix metalloproteinase 9 (MMP9), microtubule-associated protein light chain 3 (LC3) antibody, HRP goat anti-mouse secondary antibody, HRP goat anti-rabbit secondary antibody (Proteintech Group, Inc.).

    Techniques: Inhibition, Western Blot, Expressing