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camera light microscopy nikon eclipse e-2000  (Nikon)

 
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    Nikon camera light microscopy nikon eclipse e-2000
    Resazurin reduction assay (RRA) and white-light <t>microscopy</t> observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.
    Camera Light Microscopy Nikon Eclipse E 2000, 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/camera light microscopy nikon eclipse e-2000/product/Nikon
    Average 90 stars, based on 1 article reviews
    camera light microscopy nikon eclipse e-2000 - by Bioz Stars, 2026-03
    90/100 stars

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    1) Product Images from "Evaluation of the antidermatophytic activity of potassium salts of N -acylhydrazinecarbodithioates and their aminotriazole-thione derivatives"

    Article Title: Evaluation of the antidermatophytic activity of potassium salts of N -acylhydrazinecarbodithioates and their aminotriazole-thione derivatives

    Journal: Scientific Reports

    doi: 10.1038/s41598-024-54025-9

    Resazurin reduction assay (RRA) and white-light microscopy observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.
    Figure Legend Snippet: Resazurin reduction assay (RRA) and white-light microscopy observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.

    Techniques Used: Light Microscopy, Incubation, Concentration Assay, Control

    Scanning-electron microscopy showing mycelial structures of T. rubrum CBS 120358 cultured on nail fragments for 24 h at 28 °C: ( A–C ) Control without drug, ( D–F ) treatment with 2d compound at 0.5 × MIC, ( G–I ) treatment with 2d compound at 1 × MIC, ( J–L ) treatment with 2d compound at 2 × MIC. Bars: 300 μm ( A, C, E, G ); 100 μm I; 80 μm ( B, E, H, K ); 30 μm ( F, I, L ).
    Figure Legend Snippet: Scanning-electron microscopy showing mycelial structures of T. rubrum CBS 120358 cultured on nail fragments for 24 h at 28 °C: ( A–C ) Control without drug, ( D–F ) treatment with 2d compound at 0.5 × MIC, ( G–I ) treatment with 2d compound at 1 × MIC, ( J–L ) treatment with 2d compound at 2 × MIC. Bars: 300 μm ( A, C, E, G ); 100 μm I; 80 μm ( B, E, H, K ); 30 μm ( F, I, L ).

    Techniques Used: Electron Microscopy, Cell Culture, Control



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    Resazurin reduction assay (RRA) and white-light <t>microscopy</t> observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.
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    Resazurin reduction assay (RRA) and white-light microscopy observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.

    Journal: Scientific Reports

    Article Title: Evaluation of the antidermatophytic activity of potassium salts of N -acylhydrazinecarbodithioates and their aminotriazole-thione derivatives

    doi: 10.1038/s41598-024-54025-9

    Figure Lengend Snippet: Resazurin reduction assay (RRA) and white-light microscopy observation of T. rubrum CBS 120358. ( A ) Viability of germinated spores of T. rubrum measuring using RRA after 24h incubation with different concentration 2d compound. Data are expressed as mean ± S.E.M (n = 3), *p < 0.05 and **p < 0.01 vs. control. Bonnefroni test. ( B ) Germinated spores untreated with 2 d compound, ( C ) Growth of hyphae from untreated with 2d compound germinated spores after 24 h of incubation; ( D ) germinated spores treated with 2d compound (1 × MIC). ( E ) No mycelia growth from germinated spores treated with 2d compound (1 × MIC) at 24 h. Scanning objective × 40 and Eyepiece × 10 = Total magnification, × 400.

    Article Snippet: The observation using camera light microscopy (Nikon Eclipse E-2000, Nikon, Japan, with DeltaPix Camera) at a total magnification of × 400 (Scanning objective × 40 and Eyepiece × 10).

    Techniques: Light Microscopy, Incubation, Concentration Assay, Control

    Scanning-electron microscopy showing mycelial structures of T. rubrum CBS 120358 cultured on nail fragments for 24 h at 28 °C: ( A–C ) Control without drug, ( D–F ) treatment with 2d compound at 0.5 × MIC, ( G–I ) treatment with 2d compound at 1 × MIC, ( J–L ) treatment with 2d compound at 2 × MIC. Bars: 300 μm ( A, C, E, G ); 100 μm I; 80 μm ( B, E, H, K ); 30 μm ( F, I, L ).

    Journal: Scientific Reports

    Article Title: Evaluation of the antidermatophytic activity of potassium salts of N -acylhydrazinecarbodithioates and their aminotriazole-thione derivatives

    doi: 10.1038/s41598-024-54025-9

    Figure Lengend Snippet: Scanning-electron microscopy showing mycelial structures of T. rubrum CBS 120358 cultured on nail fragments for 24 h at 28 °C: ( A–C ) Control without drug, ( D–F ) treatment with 2d compound at 0.5 × MIC, ( G–I ) treatment with 2d compound at 1 × MIC, ( J–L ) treatment with 2d compound at 2 × MIC. Bars: 300 μm ( A, C, E, G ); 100 μm I; 80 μm ( B, E, H, K ); 30 μm ( F, I, L ).

    Article Snippet: The observation using camera light microscopy (Nikon Eclipse E-2000, Nikon, Japan, with DeltaPix Camera) at a total magnification of × 400 (Scanning objective × 40 and Eyepiece × 10).

    Techniques: Electron Microscopy, Cell Culture, Control