Review



spinning-disk confocal fluorescence microscopy ti2  (Nikon)


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    Structured Review

    Nikon spinning-disk confocal fluorescence microscopy ti2
    3D <t>fluorescence</t> <t>microscopy</t> 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
    Spinning Disk Confocal Fluorescence Microscopy Ti2, supplied by Nikon, 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/product/spinning-disk+confocal+fluorescence+microscopy+ti2/pmc10866835-128-14-19?v=Nikon
    Average 90 stars, based on 1 article reviews
    spinning-disk confocal fluorescence microscopy ti2 - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Anti-CD38 targeted nanotrojan horses stimulated by acoustic waves as therapeutic nanotools selectively against Burkitt’s lymphoma cells"

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

    Journal: Discover Nano

    doi: 10.1186/s11671-024-03976-z

    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
    Figure Legend 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

    Techniques Used: 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
    Figure Legend 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

    Techniques Used: Fluorescence, Microscopy



    Similar Products

    spinning-disk confocal fluorescence microscopy ti2  (Nikon)
    90
    Nikon spinning-disk confocal fluorescence microscopy ti2
    3D <t>fluorescence</t> <t>microscopy</t> 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
    Spinning Disk Confocal Fluorescence Microscopy Ti2, supplied by Nikon, 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/product/spinning-disk+confocal+fluorescence+microscopy+ti2/pmc10866835-128-14-19?v=Nikon
    Average 90 stars, based on 1 article reviews
    spinning-disk confocal fluorescence microscopy ti2 - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    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