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confocal fluorescence microscopy a1 plus  (Nikon)


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    Nikon confocal fluorescence microscopy a1 plus
    Confocal Fluorescence Microscopy A1 Plus, 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/confocal+fluorescence+microscopy+a1+plus/te2000/ppr0834286-208-21-24
    Average 90 stars, based on 1 article reviews
    confocal fluorescence microscopy a1 plus - by Bioz Stars, 2026-10
    90/100 stars

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    Article Title: hUCMSC-derived Exosomes promote spinal cord repair by alleviating the disruption of the blood-spinal cord barrier
    Article Snippet: Finally, the tissues were treated with 4′,6-diamidino-2-phenylindole (DAPI) for 10 minutes and washed with PBS, and images were captured by using confocal uorescence microscopy (Nikon, A1 PLUS, Tokyo, Japan).



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    bFGF enhances the action of SCs engulfing myelin debris in vitro. A, Schematic diagram illustrating the specific process of SCs phagocytosis of myelin debris. B, Representative images acquired by a Nikon ECLIPSE Ti <t>microscopy</t> with the phase contrast and <t>fluorescence</t> mode to record primary SCs intake of pHRODO‐labelled myelin at intervals of 6 h. Scale bar = 200 μm. C, Quantification of integrated fluorescence with the treatment indicated above. Data are shown as means ± SEM. bFGF, basic fibroblast growth factor; SC, Schwann cell. && P < 0.01 as compared to the control group
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    bFGF enhances the action of SCs engulfing myelin debris in vitro. A, Schematic diagram illustrating the specific process of SCs phagocytosis of myelin debris. B, Representative images acquired by a Nikon ECLIPSE Ti microscopy with the phase contrast and fluorescence mode to record primary SCs intake of pHRODO‐labelled myelin at intervals of 6 h. Scale bar = 200 μm. C, Quantification of integrated fluorescence with the treatment indicated above. Data are shown as means ± SEM. bFGF, basic fibroblast growth factor; SC, Schwann cell. && P < 0.01 as compared to the control group

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Basic fibroblast growth factor accelerates myelin debris clearance through activating autophagy to facilitate early peripheral nerve regeneration

    doi: 10.1111/jcmm.16274

    Figure Lengend Snippet: bFGF enhances the action of SCs engulfing myelin debris in vitro. A, Schematic diagram illustrating the specific process of SCs phagocytosis of myelin debris. B, Representative images acquired by a Nikon ECLIPSE Ti microscopy with the phase contrast and fluorescence mode to record primary SCs intake of pHRODO‐labelled myelin at intervals of 6 h. Scale bar = 200 μm. C, Quantification of integrated fluorescence with the treatment indicated above. Data are shown as means ± SEM. bFGF, basic fibroblast growth factor; SC, Schwann cell. && P < 0.01 as compared to the control group

    Article Snippet: Finally, the fluorescence images were captured using laser confocal scanning fluorescence microscopy (Nikon, A1 PLUS, Tokyo, Japan) and the fluorescent intensity was quantified with ImageJ software (National Institutes of Health, Bethesda, MD, USA).

    Techniques: In Vitro, Microscopy, Fluorescence, Control