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vegf2r  (R&D Systems)


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    Structured Review

    R&D Systems vegf2r
    Vegf2r, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/vegf2r/product/R&D Systems
    Average 92 stars, based on 21 article reviews
    vegf2r - by Bioz Stars, 2026-03
    92/100 stars

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    Image Search Results


    A) Min and Max diseased peripheral arterial segments were procured from the lower extremities of patients with severe PAD, and with or without T2D. Peripheral arterial segments were also harvested from health organ donors as controls. B-E) Western blot of CEPT1 in healthy, non-T2D Min, T2D Min, non-T2D Max, and T2D Max-diseased arterial segments was quantified relative to GAPDH (n=3-8). F-J) Immunostaining of arterial segments for CEPT1, ACOX1, VEGF2R, p-Akt, and p-eNOS that colocalized with CD31. Colocalization between two channels (fractions of CEPT1, ACOX1, VEGF2R, p-Akt, and p-eNOS colocalized with CD31) were expressed by Manders coefficients. Data are presented as mean ± SEM. * p<0.05; ** p<0.01; *** p<0.001. P values were from 1-way ANOVA and unpaired Student t -test.

    Journal: bioRxiv

    Article Title: Endothelial Cept1 Promotes Post-Ischemic Angiogenesis in a Pparα -Dependent Fashion

    doi: 10.1101/2025.03.11.642511

    Figure Lengend Snippet: A) Min and Max diseased peripheral arterial segments were procured from the lower extremities of patients with severe PAD, and with or without T2D. Peripheral arterial segments were also harvested from health organ donors as controls. B-E) Western blot of CEPT1 in healthy, non-T2D Min, T2D Min, non-T2D Max, and T2D Max-diseased arterial segments was quantified relative to GAPDH (n=3-8). F-J) Immunostaining of arterial segments for CEPT1, ACOX1, VEGF2R, p-Akt, and p-eNOS that colocalized with CD31. Colocalization between two channels (fractions of CEPT1, ACOX1, VEGF2R, p-Akt, and p-eNOS colocalized with CD31) were expressed by Manders coefficients. Data are presented as mean ± SEM. * p<0.05; ** p<0.01; *** p<0.001. P values were from 1-way ANOVA and unpaired Student t -test.

    Article Snippet: Proteins for western blot and immunostaining were detected with rabbit anti-CEPT1 (bs-12284R; Bioss USA), mouse anti-PPARα (66826-1-1g; Proteintech), rabbit anti-ACOX1 (10957-1-AP; Proteintech), rabbit anti-VEGF-A (bs-1665R; Bioss USA), rabbit anti-VEGF2r (#2472; Cell Signaling), rabbit anti-eNOS (PA1-037; Thermo Fisher), rabbit anti-p-eNOS (MA5-14957; Thermo Fisher), rabbit anti-Akt (MA5-14916; Thermo Fisher), rabbit anti-p-Akt (#9271; Cell Signaling), and mouse anti-CD31 (sc-376764; Santa Cruz Biotechnology, Inc).

    Techniques: Western Blot, Immunostaining

    A) Western blotting demonstrates that CEPT1 content is increased in ECs isolated from Cept1 fl/fl Cre + mice. Representative blots of VEGF2R, PPAR α , ACOX1, p-Akt, t-Akt and p-eNOS, t-eNOS are also provided. B) Quantitative representation of protein content relative to GAPDH as a loading control (n=3). C) RT-PCR analysis demonstrates Cept1 is overexpressed in ECs isolated from Cept1 fl/fl Cre + mice (n=3). Gene expression of Pparα, Acox1 , Vegfa, and Vegf2r is also provided (n=3). D) Western blotting demonstrates that CEPT1 content is increased in HUVECs transduced with Cept1 lentiviral particles (MOI 5). Representative blots of VEGF2R, PPAR α , ACOX1, p-AKT, t-AKT and p-eNOS, t-eNOS are also provided. E) Quantitative representation of protein content relative to GAPDH as a loading control (n=3). F) RT-PCR analysis demonstrates Cept1 is overexpressed in transduced ECs (n=3). Gene expression of Pparα, Acox1 , Vegfa, and Vegf2r is also provided (n=3). Data are presented as mean ± SEM. * p<0.05; ** p<0.01; *** p<0.001. p values were from 1-way ANOVA and unpaired Student t -test.

    Journal: bioRxiv

    Article Title: Endothelial Cept1 Promotes Post-Ischemic Angiogenesis in a Pparα -Dependent Fashion

    doi: 10.1101/2025.03.11.642511

    Figure Lengend Snippet: A) Western blotting demonstrates that CEPT1 content is increased in ECs isolated from Cept1 fl/fl Cre + mice. Representative blots of VEGF2R, PPAR α , ACOX1, p-Akt, t-Akt and p-eNOS, t-eNOS are also provided. B) Quantitative representation of protein content relative to GAPDH as a loading control (n=3). C) RT-PCR analysis demonstrates Cept1 is overexpressed in ECs isolated from Cept1 fl/fl Cre + mice (n=3). Gene expression of Pparα, Acox1 , Vegfa, and Vegf2r is also provided (n=3). D) Western blotting demonstrates that CEPT1 content is increased in HUVECs transduced with Cept1 lentiviral particles (MOI 5). Representative blots of VEGF2R, PPAR α , ACOX1, p-AKT, t-AKT and p-eNOS, t-eNOS are also provided. E) Quantitative representation of protein content relative to GAPDH as a loading control (n=3). F) RT-PCR analysis demonstrates Cept1 is overexpressed in transduced ECs (n=3). Gene expression of Pparα, Acox1 , Vegfa, and Vegf2r is also provided (n=3). Data are presented as mean ± SEM. * p<0.05; ** p<0.01; *** p<0.001. p values were from 1-way ANOVA and unpaired Student t -test.

    Article Snippet: Proteins for western blot and immunostaining were detected with rabbit anti-CEPT1 (bs-12284R; Bioss USA), mouse anti-PPARα (66826-1-1g; Proteintech), rabbit anti-ACOX1 (10957-1-AP; Proteintech), rabbit anti-VEGF-A (bs-1665R; Bioss USA), rabbit anti-VEGF2r (#2472; Cell Signaling), rabbit anti-eNOS (PA1-037; Thermo Fisher), rabbit anti-p-eNOS (MA5-14957; Thermo Fisher), rabbit anti-Akt (MA5-14916; Thermo Fisher), rabbit anti-p-Akt (#9271; Cell Signaling), and mouse anti-CD31 (sc-376764; Santa Cruz Biotechnology, Inc).

    Techniques: Western Blot, Isolation, Control, Reverse Transcription Polymerase Chain Reaction, Gene Expression, Transduction