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ecis zθ system  (Applied BioPhysics)


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    Structured Review

    Applied BioPhysics ecis zθ system
    A) hCMEC barrier resistance was assessed by <t>ECIS</t> <t>Zθ</t> to evaluate barrier integrity. Human CMEC were treated with 10µM Aβ40-Q22 (Q22), alone or in combination with 10 or 30µM 4ITP. B-C) Western blot analysis of occludin and oligomeric claudin-5 (normalized to actin, and plotted as % change of Ctrl), following 24h (B) and 48h (C) treatment. Data represents 3 individual experiments with 2 replicates per group, graphed as mean ± SEM. Statistical significance was evaluated by One-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01, ***P<0.001, ****P<0.0001
    Ecis Zθ System, supplied by Applied BioPhysics, used in various techniques. Bioz Stars score: 96/100, based on 636 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ecis+z%CE%B8+system/ECIS+Z+Theta/bio_rxiv__64898__2026__03__16__711716-163-7-10
    Average 96 stars, based on 636 article reviews
    ecis zθ system - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "Mitochondrial carbonic anhydrase-VB inhibition rescues brain endothelial stress and memory in Alzheimer’s disease models"

    Article Title: Mitochondrial carbonic anhydrase-VB inhibition rescues brain endothelial stress and memory in Alzheimer’s disease models

    Journal: bioRxiv

    doi: 10.64898/2026.03.16.711716

    A) hCMEC barrier resistance was assessed by ECIS Zθ to evaluate barrier integrity. Human CMEC were treated with 10µM Aβ40-Q22 (Q22), alone or in combination with 10 or 30µM 4ITP. B-C) Western blot analysis of occludin and oligomeric claudin-5 (normalized to actin, and plotted as % change of Ctrl), following 24h (B) and 48h (C) treatment. Data represents 3 individual experiments with 2 replicates per group, graphed as mean ± SEM. Statistical significance was evaluated by One-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01, ***P<0.001, ****P<0.0001
    Figure Legend Snippet: A) hCMEC barrier resistance was assessed by ECIS Zθ to evaluate barrier integrity. Human CMEC were treated with 10µM Aβ40-Q22 (Q22), alone or in combination with 10 or 30µM 4ITP. B-C) Western blot analysis of occludin and oligomeric claudin-5 (normalized to actin, and plotted as % change of Ctrl), following 24h (B) and 48h (C) treatment. Data represents 3 individual experiments with 2 replicates per group, graphed as mean ± SEM. Statistical significance was evaluated by One-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01, ***P<0.001, ****P<0.0001

    Techniques Used: Western Blot

    CA-VB KO in hCMEC protects from Aβ-induced apoptosis and BBB permeability . A) WB confirmed CA-VB absence in KO cells. B) DNA fragmentation, plotted as fold of change (FOC) of untreated control (ctrl) cells, measured by cell death ELISA. C) Representative IF images of active caspase-3/7 (green) and quantification to the right in CMEC treated with 25µM Q22 for 24 hours. Original magnification: 10x . D) IF of CA-VB KO vs WT hCMEC to detect mitochondrial membrane potential (Mito-tracker, red) as well as cytochrome C (Cyto C, green), in hCMEC challenged with Q22 for 16 hours. Zoom images of the merge signal at the bottom depict altered mitochondrial network with perinuclear mitochondria in Q22-treated hCMEC, but not in CA-VB KO cells. Original magnification:100x E) Mitochondrial H 2 O 2 measured with Amplex Red kit. F) Barrier resistance was measured over time with ECIS-Zθ in WT and CA-VB KO hCMEC treated or not with 10µM Q22. Data represents 3 individual experiments with 2 replicates each, graphed as mean ± SEM. Statistical significance was evaluated by Two-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01 ****P<0.0001
    Figure Legend Snippet: CA-VB KO in hCMEC protects from Aβ-induced apoptosis and BBB permeability . A) WB confirmed CA-VB absence in KO cells. B) DNA fragmentation, plotted as fold of change (FOC) of untreated control (ctrl) cells, measured by cell death ELISA. C) Representative IF images of active caspase-3/7 (green) and quantification to the right in CMEC treated with 25µM Q22 for 24 hours. Original magnification: 10x . D) IF of CA-VB KO vs WT hCMEC to detect mitochondrial membrane potential (Mito-tracker, red) as well as cytochrome C (Cyto C, green), in hCMEC challenged with Q22 for 16 hours. Zoom images of the merge signal at the bottom depict altered mitochondrial network with perinuclear mitochondria in Q22-treated hCMEC, but not in CA-VB KO cells. Original magnification:100x E) Mitochondrial H 2 O 2 measured with Amplex Red kit. F) Barrier resistance was measured over time with ECIS-Zθ in WT and CA-VB KO hCMEC treated or not with 10µM Q22. Data represents 3 individual experiments with 2 replicates each, graphed as mean ± SEM. Statistical significance was evaluated by Two-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01 ****P<0.0001

    Techniques Used: Permeability, Control, Enzyme-linked Immunosorbent Assay, Membrane

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    Expressing:

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    Image Search Results


    A) hCMEC barrier resistance was assessed by ECIS Zθ to evaluate barrier integrity. Human CMEC were treated with 10µM Aβ40-Q22 (Q22), alone or in combination with 10 or 30µM 4ITP. B-C) Western blot analysis of occludin and oligomeric claudin-5 (normalized to actin, and plotted as % change of Ctrl), following 24h (B) and 48h (C) treatment. Data represents 3 individual experiments with 2 replicates per group, graphed as mean ± SEM. Statistical significance was evaluated by One-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01, ***P<0.001, ****P<0.0001

    Journal: bioRxiv

    Article Title: Mitochondrial carbonic anhydrase-VB inhibition rescues brain endothelial stress and memory in Alzheimer’s disease models

    doi: 10.64898/2026.03.16.711716

    Figure Lengend Snippet: A) hCMEC barrier resistance was assessed by ECIS Zθ to evaluate barrier integrity. Human CMEC were treated with 10µM Aβ40-Q22 (Q22), alone or in combination with 10 or 30µM 4ITP. B-C) Western blot analysis of occludin and oligomeric claudin-5 (normalized to actin, and plotted as % change of Ctrl), following 24h (B) and 48h (C) treatment. Data represents 3 individual experiments with 2 replicates per group, graphed as mean ± SEM. Statistical significance was evaluated by One-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01, ***P<0.001, ****P<0.0001

    Article Snippet: Trans-endothelial electrical resistance was measured using the ECIS ZΘ system (Applied Biophysics).

    Techniques: Western Blot

    CA-VB KO in hCMEC protects from Aβ-induced apoptosis and BBB permeability . A) WB confirmed CA-VB absence in KO cells. B) DNA fragmentation, plotted as fold of change (FOC) of untreated control (ctrl) cells, measured by cell death ELISA. C) Representative IF images of active caspase-3/7 (green) and quantification to the right in CMEC treated with 25µM Q22 for 24 hours. Original magnification: 10x . D) IF of CA-VB KO vs WT hCMEC to detect mitochondrial membrane potential (Mito-tracker, red) as well as cytochrome C (Cyto C, green), in hCMEC challenged with Q22 for 16 hours. Zoom images of the merge signal at the bottom depict altered mitochondrial network with perinuclear mitochondria in Q22-treated hCMEC, but not in CA-VB KO cells. Original magnification:100x E) Mitochondrial H 2 O 2 measured with Amplex Red kit. F) Barrier resistance was measured over time with ECIS-Zθ in WT and CA-VB KO hCMEC treated or not with 10µM Q22. Data represents 3 individual experiments with 2 replicates each, graphed as mean ± SEM. Statistical significance was evaluated by Two-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01 ****P<0.0001

    Journal: bioRxiv

    Article Title: Mitochondrial carbonic anhydrase-VB inhibition rescues brain endothelial stress and memory in Alzheimer’s disease models

    doi: 10.64898/2026.03.16.711716

    Figure Lengend Snippet: CA-VB KO in hCMEC protects from Aβ-induced apoptosis and BBB permeability . A) WB confirmed CA-VB absence in KO cells. B) DNA fragmentation, plotted as fold of change (FOC) of untreated control (ctrl) cells, measured by cell death ELISA. C) Representative IF images of active caspase-3/7 (green) and quantification to the right in CMEC treated with 25µM Q22 for 24 hours. Original magnification: 10x . D) IF of CA-VB KO vs WT hCMEC to detect mitochondrial membrane potential (Mito-tracker, red) as well as cytochrome C (Cyto C, green), in hCMEC challenged with Q22 for 16 hours. Zoom images of the merge signal at the bottom depict altered mitochondrial network with perinuclear mitochondria in Q22-treated hCMEC, but not in CA-VB KO cells. Original magnification:100x E) Mitochondrial H 2 O 2 measured with Amplex Red kit. F) Barrier resistance was measured over time with ECIS-Zθ in WT and CA-VB KO hCMEC treated or not with 10µM Q22. Data represents 3 individual experiments with 2 replicates each, graphed as mean ± SEM. Statistical significance was evaluated by Two-way ANOVA followed by Tukey post-hoc test. *P< 0.05, **P<0.01 ****P<0.0001

    Article Snippet: Trans-endothelial electrical resistance was measured using the ECIS ZΘ system (Applied Biophysics).

    Techniques: Permeability, Control, Enzyme-linked Immunosorbent Assay, Membrane