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Nikon eclipse ti e c2 confocal laser scanning microscope
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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Danaher Inc confocal laser scanning microscope
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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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