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4-well glass-bottom imaging cell culture dishes µ-slide 4 well  (ibidi GmbH)

 
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    Structured Review

    ibidi GmbH 4-well glass-bottom imaging cell culture dishes µ-slide 4 well
    4 Well Glass Bottom Imaging Cell Culture Dishes µ Slide 4 Well, supplied by ibidi GmbH, 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/cell+imaging+dish+with+a+glass+bottom/micro+insert+4+wells/pm40011312-87-5-13
    Average 90 stars, based on 1 article reviews
    4-well glass-bottom imaging cell culture dishes µ-slide 4 well - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention.
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with Pharmaceutics 2020, 12, 1151 5 of 17 F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 ◦C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 °C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.

    Incubation:

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention.
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with Pharmaceutics 2020, 12, 1151 5 of 17 F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 ◦C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 °C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.

    Staining:

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention.
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with Pharmaceutics 2020, 12, 1151 5 of 17 F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 ◦C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.

    Article Title: Topical Delivery of Carvedilol Loaded Nano-Transfersomes for Skin Cancer Chemoprevention
    Article Snippet: F18 containing 10 μM (4 μg/mL) carvedilol, with or without being labeled with DiI, was incubated with the cells for 1, 3, 5, and 24 h. The cells were rinsed with PBS, and images were taken using an EVOS Cell Imaging System fluorescence microscope (ThermoFisher). .. The same experiment was repeated by seeding the cells on a 35 mm cell imaging dish with a glass bottom (ibidi GmbH, Gräfelfing, Germany), and cells were incubated with F18 for 3 h. After the cells were rinsed with PBS, the nuclei were stained with 5 μM Hoechst 33342 nucleic acid stain (ThermoFisher) for 20 min at 37 °C. .. The cells were then rinsed with PBS and observed using a Leica TCS SPE confocal microscope (Leica, Buffalo Grove, IL, USA) with an HC PL APO CS2 40× 1.10 NA water immersion objective.



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