Review



multi channel cytoflex s flow cytometry analyzer  (Danaher Inc)


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    Structured Review

    Danaher Inc multi channel cytoflex s flow cytometry analyzer
    ( A ) Flow <t>cytometry</t> staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
    Multi Channel Cytoflex S Flow Cytometry Analyzer, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 97/100, based on 2186 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/multi channel cytoflex s flow cytometry analyzer/product/Danaher Inc
    Average 97 stars, based on 2186 article reviews
    multi channel cytoflex s flow cytometry analyzer - by Bioz Stars, 2026-02
    97/100 stars

    Images

    1) Product Images from "Elemental Composition and Degradation Rate Impact the Biocompatibility of Copper Chalcogenide Nanocrystals"

    Article Title: Elemental Composition and Degradation Rate Impact the Biocompatibility of Copper Chalcogenide Nanocrystals

    Journal: bioRxiv

    doi: 10.64898/2025.12.17.695045

    ( A ) Flow cytometry staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
    Figure Legend Snippet: ( A ) Flow cytometry staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.

    Techniques Used: Flow Cytometry, Staining, Incubation, Concentration Assay



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    ( A ) Flow <t>cytometry</t> staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
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    ( A ) Flow <t>cytometry</t> staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
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    ( A ) Flow <t>cytometry</t> staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
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    ( A ) Flow <t>cytometry</t> staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.
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    Image Search Results


    ( A ) Flow cytometry staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.

    Journal: bioRxiv

    Article Title: Elemental Composition and Degradation Rate Impact the Biocompatibility of Copper Chalcogenide Nanocrystals

    doi: 10.64898/2025.12.17.695045

    Figure Lengend Snippet: ( A ) Flow cytometry staining of HepG 2 cells with apoptosis and necrosis indicators Apopxin Red and Nuclear Green DSC1, respectively, following 6 hr incubation with 150 µg/mL copper chalcogenide NCs (cation concentration). ( B ). Summary and statistical analysis of the necrosis assay (n = 3). * p < 0.05, **** p < 0.0001.

    Article Snippet: The cells were measured using a multi-channel CytoFLEX S flow cytometry analyzer (Beckman Coulter, CA, USA).

    Techniques: Flow Cytometry, Staining, Incubation, Concentration Assay