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c2 laser scanning confocal microscope  (Nikon)


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    Structured Review

    Nikon c2 laser scanning confocal microscope
    C2 Laser Scanning Confocal Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c2 laser scanning confocal microscope/product/Nikon
    Average 99 stars, based on 1 article reviews
    c2 laser scanning confocal microscope - by Bioz Stars, 2026-06
    99/100 stars

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    Colony and biofilm calcofluor staining assays. Production of exopolysaccharide (EPS) by the wild-type ( A. brasilense Sp7), the cysK-A mutant ( A. brasilense AR), and the complemented ( A . brasilense AR-pAB- cysK ) strains were visualized by staining with calcofluor, which binds to β-linked polysaccharides. ( A ) Colonies were grown for 5 days at 30 °C on solid LB medium (lacking NaCl) supplemented with Calcofluor (200 μg/mL). Images were captured under UV illumination to visualize fluorescence. Scale bar = 10 mm. ( B ) Confocal micrographs of biofilms grown for 5 days at 30 °C on agar-solidified Nfb∗ medium containing Calcofluor (85 μM). The biofilms were observed with a Nikon <t>Eclipse</t> <t>Ti-E</t> <t>C2+</t> <t>microscope.</t> Scale bar = 20 μm.
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    Characterization of nanoplatforms. (A) Particle size distribution and Transmission electron <t>microscope</t> (TEM) image of PSSQ micelles. (B) Critical micellar concentration (CMC) of PSSQ micelles. (C-E) Changes of particle size and TEM image of PSSQ micelles in different media. Particle size and TEM image of (F) TLP and (G) PSSQ@TLP. (H) Cumulative release profiles of SN38 from PSSQ@TLP in different release media ( n = 3). (I) Storage stability of PSSQ@TLP in phosphate-buffered saline (PBS) (pH 7.4) at 37 °C (evaluated by particle size and PDI changes, data are shown as mean ± SD, n = 3).
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    Image Search Results


    Colony and biofilm calcofluor staining assays. Production of exopolysaccharide (EPS) by the wild-type ( A. brasilense Sp7), the cysK-A mutant ( A. brasilense AR), and the complemented ( A . brasilense AR-pAB- cysK ) strains were visualized by staining with calcofluor, which binds to β-linked polysaccharides. ( A ) Colonies were grown for 5 days at 30 °C on solid LB medium (lacking NaCl) supplemented with Calcofluor (200 μg/mL). Images were captured under UV illumination to visualize fluorescence. Scale bar = 10 mm. ( B ) Confocal micrographs of biofilms grown for 5 days at 30 °C on agar-solidified Nfb∗ medium containing Calcofluor (85 μM). The biofilms were observed with a Nikon Eclipse Ti-E C2+ microscope. Scale bar = 20 μm.

    Journal: Biofilm

    Article Title: Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7

    doi: 10.1016/j.bioflm.2025.100335

    Figure Lengend Snippet: Colony and biofilm calcofluor staining assays. Production of exopolysaccharide (EPS) by the wild-type ( A. brasilense Sp7), the cysK-A mutant ( A. brasilense AR), and the complemented ( A . brasilense AR-pAB- cysK ) strains were visualized by staining with calcofluor, which binds to β-linked polysaccharides. ( A ) Colonies were grown for 5 days at 30 °C on solid LB medium (lacking NaCl) supplemented with Calcofluor (200 μg/mL). Images were captured under UV illumination to visualize fluorescence. Scale bar = 10 mm. ( B ) Confocal micrographs of biofilms grown for 5 days at 30 °C on agar-solidified Nfb∗ medium containing Calcofluor (85 μM). The biofilms were observed with a Nikon Eclipse Ti-E C2+ microscope. Scale bar = 20 μm.

    Article Snippet: After five days of static incubation at 30 °C, three-dimensional biofilm structures were observed using an Eclipse Ti-E C2+ confocal laser scanning microscope (Nikon) equipped with CFI Plan Apo VC 20x/1.2 and CFI Plan Apo VC 60x/1.2 WI objective lenses.

    Techniques: Staining, Mutagenesis, Fluorescence, Microscopy

    Characterization of nanoplatforms. (A) Particle size distribution and Transmission electron microscope (TEM) image of PSSQ micelles. (B) Critical micellar concentration (CMC) of PSSQ micelles. (C-E) Changes of particle size and TEM image of PSSQ micelles in different media. Particle size and TEM image of (F) TLP and (G) PSSQ@TLP. (H) Cumulative release profiles of SN38 from PSSQ@TLP in different release media ( n = 3). (I) Storage stability of PSSQ@TLP in phosphate-buffered saline (PBS) (pH 7.4) at 37 °C (evaluated by particle size and PDI changes, data are shown as mean ± SD, n = 3).

    Journal: International Journal of Pharmaceutics: X

    Article Title: Encapsulating GSH/NQO1-responsive SN38 prodrug micelles with Timosaponin AIII-based multifunctional liposomes for tumor-targeted chemotherapy

    doi: 10.1016/j.ijpx.2026.100497

    Figure Lengend Snippet: Characterization of nanoplatforms. (A) Particle size distribution and Transmission electron microscope (TEM) image of PSSQ micelles. (B) Critical micellar concentration (CMC) of PSSQ micelles. (C-E) Changes of particle size and TEM image of PSSQ micelles in different media. Particle size and TEM image of (F) TLP and (G) PSSQ@TLP. (H) Cumulative release profiles of SN38 from PSSQ@TLP in different release media ( n = 3). (I) Storage stability of PSSQ@TLP in phosphate-buffered saline (PBS) (pH 7.4) at 37 °C (evaluated by particle size and PDI changes, data are shown as mean ± SD, n = 3).

    Article Snippet: Cells were washed with saline, fixed with 4% paraformaldehyde, stained with DAPI, and imaged using a confocal laser scanning microscope (CLSM, STELLARIS 5, Leica, Germany).

    Techniques: Transmission Assay, Microscopy, Concentration Assay, Saline