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dead cell stain 2% ethidium homodimer-1 e1169  (Thermo Fisher)


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    Thermo Fisher dead cell stain 2% ethidium homodimer-1 e1169
    Dead Cell Stain 2% Ethidium Homodimer 1 E1169, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dead cell stain 2% ethidium homodimer-1 e1169/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    dead cell stain 2% ethidium homodimer-1 e1169 - by Bioz Stars, 2026-02
    90/100 stars

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    Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = <t>green,</t> <t>EthD-1</t> = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).
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    Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = <t>green,</t> <t>EthD-1</t> = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).
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    Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = <t>green,</t> <t>EthD-1</t> = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).
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    Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = <t>green,</t> <t>EthD-1</t> = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).
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    Image Search Results


    Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = green, EthD-1 = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).

    Journal: Scientific Reports

    Article Title: A perfusable decellularized plant-based air-liquid-interface-on-a-chip for investigating inorganic dust aerosol exposure

    doi: 10.1038/s41598-025-33930-7

    Figure Lengend Snippet: Diagram of air–liquid-interface platform for dust exposure. ( A ) Stepwise experimental timeline of the decellularized plant-based ALI model and dust exposure. ( B ) 3D design of the platform, which provides an enclosed chamber for accommodating spinach leaves. ( C ) The macroscopic image of the recellularized spinach integrated into the air–liquid-interface platform. Live/Dead fluorescence images (Calcein-AM = green, EthD-1 = red) of recellularized leaves (Left and right panels correspond to images taken from different focal planes representing the apical epithelial surface and the vascular endothelial layer, respectively). ( D ) Quantitative cell viability of BEAS-2B and HUVECs analyzed using ImageJ software (NIH, USA).

    Article Snippet: Cell viability within the recellularized spinach scaffolds was evaluated using a Calcein-AM/Ethidium homodimer-1 (EthD-1) Live/Dead Viability/Cytotoxicity Kit (Biotium, USA) following the manufacturer’s protocol.

    Techniques: Fluorescence, Software