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mouse brain microvascular ecs  (AcceGen Biotechnology)


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    Structured Review

    AcceGen Biotechnology mouse brain microvascular ecs
    Mouse Brain Microvascular Ecs, supplied by AcceGen Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+brain+microvascular+ecs/pmc12052699-35-3-7?v=AcceGen+Biotechnology
    Average 93 stars, based on 1 article reviews
    mouse brain microvascular ecs - by Bioz Stars, 2026-07
    93/100 stars

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    EPC-EXs derived from R+ mice are less effective on rescuing ECs from Ang II plus H/R-induced apoptosis and compromised cell viability. (A) representative plots, and summarized data of cell apoptosis. (B) cleaved cas-3/β-actin expression in ECs co-cultured with the two types of EPC-EXs. (C) cell viability of ECs co-cultured with the two types of EPC-EXs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain <t>microvascular</t> ECs (Cell Biologics) subjected to Ang II (10–6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.
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    EPC-EXs derived from R+ mice are less effective on rescuing ECs from Ang II plus H/R-induced apoptosis and compromised cell viability. (A) representative plots, and summarized data of cell apoptosis. (B) cleaved cas-3/β-actin expression in ECs co-cultured with the two types of EPC-EXs. (C) cell viability of ECs co-cultured with the two types of EPC-EXs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain <t>microvascular</t> ECs (Cell Biologics) subjected to Ang II (10–6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.
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    EPC-EXs derived from R+ mice are less effective on rescuing ECs from Ang II plus H/R-induced apoptosis and compromised cell viability. (A) representative plots, and summarized data of cell apoptosis. (B) cleaved cas-3/β-actin expression in ECs co-cultured with the two types of EPC-EXs. (C) cell viability of ECs co-cultured with the two types of EPC-EXs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain <t>microvascular</t> ECs (Cell Biologics) subjected to Ang II (10–6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.
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    Image Search Results


    EPC-EXs derived from R+ mice are less effective on rescuing ECs from Ang II plus H/R-induced apoptosis and compromised cell viability. (A) representative plots, and summarized data of cell apoptosis. (B) cleaved cas-3/β-actin expression in ECs co-cultured with the two types of EPC-EXs. (C) cell viability of ECs co-cultured with the two types of EPC-EXs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain microvascular ECs (Cell Biologics) subjected to Ang II (10–6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.

    Journal: Frontiers in stroke

    Article Title: Compromised endothelial progenitor cell exosomal communication with endothelial cells in hypertension ischemia conditions

    doi: 10.3389/fstro.2022.1015463

    Figure Lengend Snippet: EPC-EXs derived from R+ mice are less effective on rescuing ECs from Ang II plus H/R-induced apoptosis and compromised cell viability. (A) representative plots, and summarized data of cell apoptosis. (B) cleaved cas-3/β-actin expression in ECs co-cultured with the two types of EPC-EXs. (C) cell viability of ECs co-cultured with the two types of EPC-EXs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain microvascular ECs (Cell Biologics) subjected to Ang II (10–6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.

    Article Snippet: A mouse brain microvascular ECs (Cell Biologics, Inc; Cat # C57–6023) were used in this study.

    Techniques: Derivative Assay, Expressing, Cell Culture, Control

    EPC-EXs derived from R+ mice are less effective in improving the tube formation ability of Ang II plus H/R-injured ECs. (A,B) representative images and summarized data showing the tube formation ability of ECs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain microvascular ECs (Cell Biologics) subjected to Ang II (10 −6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.

    Journal: Frontiers in stroke

    Article Title: Compromised endothelial progenitor cell exosomal communication with endothelial cells in hypertension ischemia conditions

    doi: 10.3389/fstro.2022.1015463

    Figure Lengend Snippet: EPC-EXs derived from R+ mice are less effective in improving the tube formation ability of Ang II plus H/R-injured ECs. (A,B) representative images and summarized data showing the tube formation ability of ECs. * p < 0.05, vs. control; + p < 0.05, vs. vehicle; $ p < 0.05, vs. WT-EPC-EXs. Data expressed as mean ± SEM, n = 6/group. EC+AngII+H/R: Mouse brain microvascular ECs (Cell Biologics) subjected to Ang II (10 −6 M) plus hypoxia/reoxygenation (H/R) injury. Primary EC+H/R: primary brain microvascular ECs from R+ mice subjected to H/R injury. Control cells were cultured in normal conditions.

    Article Snippet: A mouse brain microvascular ECs (Cell Biologics, Inc; Cat # C57–6023) were used in this study.

    Techniques: Derivative Assay, Control, Cell Culture