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eclipse ti2 spinning disk confocal microscopy system  (Nikon)


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    Nikon eclipse ti2 spinning disk confocal microscopy system
    Eclipse Ti2 Spinning Disk Confocal Microscopy System, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 10098 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/eclipse ti2 spinning disk confocal microscopy system/product/Nikon
    Average 99 stars, based on 10098 article reviews
    eclipse ti2 spinning disk confocal microscopy system - by Bioz Stars, 2026-05
    99/100 stars

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    3D fluorescence microscopy images of Daudi ( a ) and lymphocytes ( d ) control cells, Daudi treated with ZnO-Lip ( b ) and ZnO-LipCD38 ( c ) and lymphocytes treated with ZnO-Lip ( e ) and ZnO-LipCD38 ( f ) after 24 h. Liposome containing ZnO NCs were labelled with DiD (red channel); cell nuclei were labelled with Hoechst (blue channel); cell membranes were labelled with WGA488 (green channel). Cells were treated with 40 μg/mL

    Journal: Discover Nano

    Article Title: Anti-CD38 targeted nanotrojan horses stimulated by acoustic waves as therapeutic nanotools selectively against Burkitt’s lymphoma cells

    doi: 10.1186/s11671-024-03976-z

    Figure Lengend Snippet: 3D fluorescence microscopy images of Daudi ( a ) and lymphocytes ( d ) control cells, Daudi treated with ZnO-Lip ( b ) and ZnO-LipCD38 ( c ) and lymphocytes treated with ZnO-Lip ( e ) and ZnO-LipCD38 ( f ) after 24 h. Liposome containing ZnO NCs were labelled with DiD (red channel); cell nuclei were labelled with Hoechst (blue channel); cell membranes were labelled with WGA488 (green channel). Cells were treated with 40 μg/mL

    Article Snippet: Internalization of ZnO-Lip and ZnO-LipCD38 on Daudi and Lymphocyte cells was evaluated also through spinning-disk confocal fluorescence microscopy (Ti2 Nikon equipped with Crest Large FOV laser and 60 × PlanAPO objective, NA = 1.40).

    Techniques: Fluorescence, Microscopy, Control

    Fluorescence microscopy images of the internalization and colocalization of ZnO-LipCD38 nanoconstruct on Daudi and lymphocytes after 24 h. Liposome containing ZnO NCs were labelled with DiD (red channel); antiCD38 fragments incorporated in the lipidic shell contained ZnO NCs were labelled with Curcumin (blue channel); cell membranes were labelled with WGA488 (green channel). Cells were treated with 40 μg/mL. White circles represent highly relevant internalization events in cells

    Journal: Discover Nano

    Article Title: Anti-CD38 targeted nanotrojan horses stimulated by acoustic waves as therapeutic nanotools selectively against Burkitt’s lymphoma cells

    doi: 10.1186/s11671-024-03976-z

    Figure Lengend Snippet: Fluorescence microscopy images of the internalization and colocalization of ZnO-LipCD38 nanoconstruct on Daudi and lymphocytes after 24 h. Liposome containing ZnO NCs were labelled with DiD (red channel); antiCD38 fragments incorporated in the lipidic shell contained ZnO NCs were labelled with Curcumin (blue channel); cell membranes were labelled with WGA488 (green channel). Cells were treated with 40 μg/mL. White circles represent highly relevant internalization events in cells

    Article Snippet: Internalization of ZnO-Lip and ZnO-LipCD38 on Daudi and Lymphocyte cells was evaluated also through spinning-disk confocal fluorescence microscopy (Ti2 Nikon equipped with Crest Large FOV laser and 60 × PlanAPO objective, NA = 1.40).

    Techniques: Fluorescence, Microscopy