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human coronary artery smooth muscle cells  (Cell Applications Inc)


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    Cell Applications Inc human coronary artery smooth muscle cells
    Human Coronary Artery Smooth Muscle Cells, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 95/100, based on 93 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human coronary artery smooth muscle cells/product/Cell Applications Inc
    Average 95 stars, based on 93 article reviews
    human coronary artery smooth muscle cells - by Bioz Stars, 2026-05
    95/100 stars

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    Cell Applications Inc p re ss human coronary artery smooth muscle cells
    In vitro biocompatibility and intracellular NO generation characterisation of DSENO materials. (a, b) Cell viability of HUVECs (a) and <t>HCASMCs</t> (b) after 48 h incubation with printed DSENO plates. (c) Quantitative analysis of material‐induced intracellular NO generation. Endogenous NO production in HUVECs was quantified by measuring the mean fluorescence intensity (MFI) of the DAF‐FM probe using high‐resolution confocal laser scanning microscopy (CLSM). (d) CLSM images of HUVECs after 48 h incubation with material candidates, cells stained with DAF‐FM (green) and Hoechst (blue) ( n ≥ 6). Scale bar = 100 µm. Data are normalized to the blank control and represent the average MFI of multiple regions of interest. Error bars indicate standard deviation; statistical significance was determined via one‐way ANOVA ( * p < 0.05).
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    In vitro biocompatibility and intracellular NO generation characterisation of DSENO materials. (a, b) Cell viability of HUVECs (a) and HCASMCs (b) after 48 h incubation with printed DSENO plates. (c) Quantitative analysis of material‐induced intracellular NO generation. Endogenous NO production in HUVECs was quantified by measuring the mean fluorescence intensity (MFI) of the DAF‐FM probe using high‐resolution confocal laser scanning microscopy (CLSM). (d) CLSM images of HUVECs after 48 h incubation with material candidates, cells stained with DAF‐FM (green) and Hoechst (blue) ( n ≥ 6). Scale bar = 100 µm. Data are normalized to the blank control and represent the average MFI of multiple regions of interest. Error bars indicate standard deviation; statistical significance was determined via one‐way ANOVA ( * p < 0.05).

    Journal: Advanced Materials (Deerfield Beach, Fla.)

    Article Title: Deployable 3D‐Printed Vascular Stent with Surface‐Catalysed Endogenous Nitric Oxide Generation

    doi: 10.1002/adma.202520199

    Figure Lengend Snippet: In vitro biocompatibility and intracellular NO generation characterisation of DSENO materials. (a, b) Cell viability of HUVECs (a) and HCASMCs (b) after 48 h incubation with printed DSENO plates. (c) Quantitative analysis of material‐induced intracellular NO generation. Endogenous NO production in HUVECs was quantified by measuring the mean fluorescence intensity (MFI) of the DAF‐FM probe using high‐resolution confocal laser scanning microscopy (CLSM). (d) CLSM images of HUVECs after 48 h incubation with material candidates, cells stained with DAF‐FM (green) and Hoechst (blue) ( n ≥ 6). Scale bar = 100 µm. Data are normalized to the blank control and represent the average MFI of multiple regions of interest. Error bars indicate standard deviation; statistical significance was determined via one‐way ANOVA ( * p < 0.05).

    Article Snippet: Human coronary artery smooth muscle cells (HCASMCs) from Cell Applications were maintained in human smooth muscle cell growth medium (311–500) and passaged at 70–90% confluency.

    Techniques: In Vitro, Incubation, Fluorescence, Confocal Laser Scanning Microscopy, Staining, Control, Standard Deviation