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a1 nikon confocal laser scanning unit  (Nikon)


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    Structured Review

    Nikon a1 nikon confocal laser scanning unit
    Aggregates of <t>PET</t> <t>NPs</t> powder visualized in brightfield (A) and confocal microscopy (B) by a 405 nm laser line of <t>A1</t> NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. Objective used 20X. Images representative of n = 3 independent experiments.
    A1 Nikon Confocal Laser Scanning Unit, 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/a1+confocal+scan+unit/pmc12183297-71-56-57?v=Nikon
    Average 90 stars, based on 1 article reviews
    a1 nikon confocal laser scanning unit - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Impact of polyethylene terephthalate nanoplastics (PET) on fibroblasts: a study on NIH-3T3 cells"

    Article Title: Impact of polyethylene terephthalate nanoplastics (PET) on fibroblasts: a study on NIH-3T3 cells

    Journal: Frontiers in Physiology

    doi: 10.3389/fphys.2025.1580682

    Aggregates of PET NPs powder visualized in brightfield (A) and confocal microscopy (B) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. Objective used 20X. Images representative of n = 3 independent experiments.
    Figure Legend Snippet: Aggregates of PET NPs powder visualized in brightfield (A) and confocal microscopy (B) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. Objective used 20X. Images representative of n = 3 independent experiments.

    Techniques Used: Confocal Microscopy, Microscopy

    Representative image (of n = 3 independent experiments) of a 3T3 fibroblast exposed to PET NPs (50 μg/mL) for 24 h visualized in brightfield (C) and confocal microscopy (D) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. A control cell (A,B) is shown for comparison. Objective used 60X oil immersion. (E) % of cells internalizing PET NPs at different NP concentrations (data are expressed as mean ± SEM of three independent experiment).
    Figure Legend Snippet: Representative image (of n = 3 independent experiments) of a 3T3 fibroblast exposed to PET NPs (50 μg/mL) for 24 h visualized in brightfield (C) and confocal microscopy (D) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. A control cell (A,B) is shown for comparison. Objective used 60X oil immersion. (E) % of cells internalizing PET NPs at different NP concentrations (data are expressed as mean ± SEM of three independent experiment).

    Techniques Used: Confocal Microscopy, Microscopy, Control, Comparison



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    Image Search Results


    Aggregates of PET NPs powder visualized in brightfield (A) and confocal microscopy (B) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. Objective used 20X. Images representative of n = 3 independent experiments.

    Journal: Frontiers in Physiology

    Article Title: Impact of polyethylene terephthalate nanoplastics (PET) on fibroblasts: a study on NIH-3T3 cells

    doi: 10.3389/fphys.2025.1580682

    Figure Lengend Snippet: Aggregates of PET NPs powder visualized in brightfield (A) and confocal microscopy (B) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. Objective used 20X. Images representative of n = 3 independent experiments.

    Article Snippet: NIH-3T3 cells (concentrated 2 × 10 4 per ml) were seeded in a tissue culture-treated μ-Slide 4 well (Ibidi GmbH, Gräfelfing, Germany) for 24 h and then they were incubated with PET NPs for 24 h. After incubation cells were washed three times to remove NPs and were visualized by a 405 nm laser line of A1 NIKON confocal laser scanning unit using coupled with a NIKON Ti microscope.

    Techniques: Confocal Microscopy, Microscopy

    Representative image (of n = 3 independent experiments) of a 3T3 fibroblast exposed to PET NPs (50 μg/mL) for 24 h visualized in brightfield (C) and confocal microscopy (D) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. A control cell (A,B) is shown for comparison. Objective used 60X oil immersion. (E) % of cells internalizing PET NPs at different NP concentrations (data are expressed as mean ± SEM of three independent experiment).

    Journal: Frontiers in Physiology

    Article Title: Impact of polyethylene terephthalate nanoplastics (PET) on fibroblasts: a study on NIH-3T3 cells

    doi: 10.3389/fphys.2025.1580682

    Figure Lengend Snippet: Representative image (of n = 3 independent experiments) of a 3T3 fibroblast exposed to PET NPs (50 μg/mL) for 24 h visualized in brightfield (C) and confocal microscopy (D) by a 405 nm laser line of A1 NIKON confocal laser scanning unit coupled with a NIKON Ti microscope. A control cell (A,B) is shown for comparison. Objective used 60X oil immersion. (E) % of cells internalizing PET NPs at different NP concentrations (data are expressed as mean ± SEM of three independent experiment).

    Article Snippet: NIH-3T3 cells (concentrated 2 × 10 4 per ml) were seeded in a tissue culture-treated μ-Slide 4 well (Ibidi GmbH, Gräfelfing, Germany) for 24 h and then they were incubated with PET NPs for 24 h. After incubation cells were washed three times to remove NPs and were visualized by a 405 nm laser line of A1 NIKON confocal laser scanning unit using coupled with a NIKON Ti microscope.

    Techniques: Confocal Microscopy, Microscopy, Control, Comparison