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eclipse te2000 s c1si laser scanning confocal microscope  (Nikon)


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    Structured Review

    Nikon eclipse te2000 s c1si laser scanning confocal microscope
    Eclipse Te2000 S C1si Laser Scanning Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59420 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+te2000+s+c1si+laser+scanning+confocal+microscope/Objectives/10__1021_slash_acsanm__5c03728-139-7-6
    Average 99 stars, based on 59420 article reviews
    eclipse te2000 s c1si laser scanning confocal microscope - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Irradiation:

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. After each irradiation, cells were stained with viability/ cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope using a 20x/0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. After each irradiation, cells were stained with viability/cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope using a 20 x /0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Staining:

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. After each irradiation, cells were stained with viability/ cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope using a 20x/0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. After each irradiation, cells were stained with viability/cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope using a 20 x /0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. Migrated cells were fixed with 4% paraformaldehyde for 15 min and stained with 25 μg/mL Hoechst for 15 min. Migrated cells were visualized under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope (Nikon, Japan) with a 20× objective. ..

    Article Title: Upconversion Nanoparticle Loaded with Chlorin e6 in a Lipid Shell for NIR Excitation-Based Photodynamic Cancer Therapy
    Article Snippet: Photodynamic therapy (PDT) is a clinically approved method for noninvasive cancer treatment with fewer side effects, high spatial resolution, low cost, and fast recovery time.. However, the penetration depth of the excitation light has significantly restricted the advancement of PDT.. Recently, upconverting nanoparticles have been suggested to extend the excitation spectrum of photosensitizers via luminescence resonance energy transfer (LRET).

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. Migrated cells were fixed with 4% paraformaldehyde for 15 min and stained with 25 μg/mL Hoechst for 15 min. Migrated cells were visualized under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope (Nikon, Japan) with a 20× objective. ..

    Fluorescence:

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. After each irradiation, cells were stained with viability/ cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope using a 20x/0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. After each irradiation, cells were stained with viability/cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope using a 20 x /0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Microscopy:

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. After each irradiation, cells were stained with viability/ cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope using a 20x/0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. After each irradiation, cells were stained with viability/cytotoxicity dyes, i.e., 2 μM calcein-AM (green fluorescence, stains viable cells) and 4 μM propidium iodide (red fluorescence, stains nonviable cells) (ROTH, Germany) and examined under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope using a 20 x /0.5 NA objective (Nikon, Japan). .. The photodynamic effect was evaluated by counting viable and nonviable cells using ImageJ software.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: .. Migrated cells were fixed with 4% paraformaldehyde for 15 min and stained with 25 μg/mL Hoechst for 15 min. Migrated cells were visualized under a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope (Nikon, Japan) with a 20× objective. ..

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles.
    Article Snippet: Eventually, the cover glass was mounted with Cytoseal 60 mounting medium (Thermo Fisher Scientific, UK). .. Intracellular accumulation of the dNP-Ce6 complex in cells was evaluated with a Nikon Eclipse Te2000−S C1si laser scanning confocal microscope (Nikon, Japan) using a 60× NA 1.4 oil immersion objective (Plan Apo, Nikon, Japan). .. A 404 nm diode laser (Melles Griot, USA) was used to excite Hoechst 33342 and Ce6, a 488 nm Ar laser (Melles Griot, USA) for Alexa Fluor 488 Phalloidin and a 980 nm laser (Changchun New Industries Optoelectronics Tech.

    Article Title: Upconversion Nanoparticle Loaded with Chlorin e6 in a Lipid Shell for NIR Excitation-Based Photodynamic Cancer Therapy
    Article Snippet: Photodynamic therapy (PDT) is a clinically approved method for noninvasive cancer treatment with fewer side effects, high spatial resolution, low cost, and fast recovery time.. However, the penetration depth of the excitation light has significantly restricted the advancement of PDT.. Recently, upconverting nanoparticles have been suggested to extend the excitation spectrum of photosensitizers via luminescence resonance energy transfer (LRET).

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: Eventually, the cover glass was mounted with Cytoseal 60 mounting medium (Thermo Fisher Scientific, UK). .. Intracellular accumulation of the dNP-Ce6 complex in cells was evaluated with a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope (Nikon, Japan) using a 60× NA 1.4 oil immersion objective (Plan Apo, Nikon, Japan). .. A 404 nm diode laser (Melles Griot, USA) was used to excite Hoechst 33342 and Ce 6 , a 488 nm Ar laser (Melles Griot, USA) for Alexa Fluor 488 Phalloidin and a 980 nm laser (Changchun New Industries Optoelectronics Tech.

    Article Title: Synergistic Enhancement of Photodynamic Cancer Therapy with Mesenchymal Stem Cells and Theranostic Nanoparticles
    Article Snippet: .. Migrated cells were fixed with 4% paraformaldehyde for 15 min and stained with 25 μg/mL Hoechst for 15 min. Migrated cells were visualized under a Nikon Eclipse Te2000–S C1si laser scanning confocal microscope (Nikon, Japan) with a 20× objective. ..



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