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inverted fluorescence microscope using a 20× objective nikon eclipse t i -s  (Nikon)

 
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    Nikon inverted fluorescence microscope using a 20× objective nikon eclipse t i -s
    Inverted Fluorescence Microscope Using A 20× Objective Nikon Eclipse T I S, 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/result/inverted fluorescence microscope using a 20× objective nikon eclipse t i -s/product/Nikon
    Average 90 stars, based on 1 article reviews
    inverted fluorescence microscope using a 20× objective nikon eclipse t i -s - by Bioz Stars, 2026-03
    90/100 stars

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    4T1 cells stained with dual staining AO/PI following treatment with 80% methanol extract for 72 hours. The cells were viewed under inverted research <t>fluorescence</t> <t>microscope</t> (Nikon ECLIPSE T i -S, Shinagawa-ku, Tokyo, Japan) at 20x magnification. (a) Control (untreated 4T1 cells) being majorly viable and uniform in shape. Green fluorescent colour indicates cells are viable. (b) 4T1 cells treated with 42.26 μ g/mL of 80% methanol extract. Red colour indicates cells that had undergone necrosis while orange colour indicates cells that had undergone apoptosis. Number of viable cells was reduced and cells were showing shrinkage. Scale bars represent 100 μ m.
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    https://www.bioz.com/result/inverted fluorescence microscope nikon eclipse t i -s/product/Nikon
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    inverted fluorescence microscope nikon eclipse t i -s - by Bioz Stars, 2026-03
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    4T1 cells stained with dual staining AO/PI following treatment with 80% methanol extract for 72 hours. The cells were viewed under inverted research fluorescence microscope (Nikon ECLIPSE T i -S, Shinagawa-ku, Tokyo, Japan) at 20x magnification. (a) Control (untreated 4T1 cells) being majorly viable and uniform in shape. Green fluorescent colour indicates cells are viable. (b) 4T1 cells treated with 42.26 μ g/mL of 80% methanol extract. Red colour indicates cells that had undergone necrosis while orange colour indicates cells that had undergone apoptosis. Number of viable cells was reduced and cells were showing shrinkage. Scale bars represent 100 μ m.

    Journal: Evidence-based Complementary and Alternative Medicine : eCAM

    Article Title: Cytotoxicity and Apoptosis Induction of Ardisia crispa and Its Solvent Partitions against Mus musculus Mammary Carcinoma Cell Line (4T1)

    doi: 10.1155/2017/9368079

    Figure Lengend Snippet: 4T1 cells stained with dual staining AO/PI following treatment with 80% methanol extract for 72 hours. The cells were viewed under inverted research fluorescence microscope (Nikon ECLIPSE T i -S, Shinagawa-ku, Tokyo, Japan) at 20x magnification. (a) Control (untreated 4T1 cells) being majorly viable and uniform in shape. Green fluorescent colour indicates cells are viable. (b) 4T1 cells treated with 42.26 μ g/mL of 80% methanol extract. Red colour indicates cells that had undergone necrosis while orange colour indicates cells that had undergone apoptosis. Number of viable cells was reduced and cells were showing shrinkage. Scale bars represent 100 μ m.

    Article Snippet: The slides were viewed under inverted research fluorescence microscope (Nikon ECLIPSE T i -S, Shinagawa-ku, Tokyo, Japan) at 20x magnification.

    Techniques: Staining, Fluorescence, Microscopy, Control