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fluorescence microscope with ds-ri2 camera  (Nikon)


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    Structured Review

    Nikon fluorescence microscope with ds-ri2 camera
    Fluorescence Microscope With Ds Ri2 Camera, 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/fluorescence+microscope+with+ds-ri2+camera/pmc10744278-158-62-6
    Average 90 stars, based on 1 article reviews
    fluorescence microscope with ds-ri2 camera - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Fluorescence:

    Article Title: Inhibiting Intracellular α 2C -Adrenoceptor Surface Translocation Using Decoy Peptides: Identification of an Essential Role of the C-Terminus in Receptor Trafficking
    Article Snippet: Cells were visualized using fluorescence microscopy (Nikon Eclipse T i 2 fluorescence microscope with DS-Ri2 camera, Nikon Corporation, Tokyo, Japan), and the mean fluorescence intensity of the surface HA- or GFP-tagged or endogenous α 2 -adrenoceptors at the cell boundary was quantitated by Nikon NIS Elements software (version 5.10) and the region of interest (ROI) tool at 4–6 random ROI on the cell boundary per cell.

    Microscopy:

    Article Title: Inhibiting Intracellular α 2C -Adrenoceptor Surface Translocation Using Decoy Peptides: Identification of an Essential Role of the C-Terminus in Receptor Trafficking
    Article Snippet: Cells were visualized using fluorescence microscopy (Nikon Eclipse T i 2 fluorescence microscope with DS-Ri2 camera, Nikon Corporation, Tokyo, Japan), and the mean fluorescence intensity of the surface HA- or GFP-tagged or endogenous α 2 -adrenoceptors at the cell boundary was quantitated by Nikon NIS Elements software (version 5.10) and the region of interest (ROI) tool at 4–6 random ROI on the cell boundary per cell.

    Software:

    Article Title: Inhibiting Intracellular α 2C -Adrenoceptor Surface Translocation Using Decoy Peptides: Identification of an Essential Role of the C-Terminus in Receptor Trafficking
    Article Snippet: Cells were visualized using fluorescence microscopy (Nikon Eclipse T i 2 fluorescence microscope with DS-Ri2 camera, Nikon Corporation, Tokyo, Japan), and the mean fluorescence intensity of the surface HA- or GFP-tagged or endogenous α 2 -adrenoceptors at the cell boundary was quantitated by Nikon NIS Elements software (version 5.10) and the region of interest (ROI) tool at 4–6 random ROI on the cell boundary per cell.



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