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bio rad zoe fluorescent cell imager  (Bio-Rad)


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    Bio-Rad bio rad zoe fluorescent cell imager
    Bio Rad Zoe Fluorescent Cell Imager, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1395 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/zoe+fluorescent+cell+imager/ZOE+Fluorescent+Cell+Imager/pm42121903-102-18-18
    Average 96 stars, based on 1395 article reviews
    bio rad zoe fluorescent cell imager - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Fluorescence:

    Article Title: Autophagy-related protein 1 orchestrates autophagy initiation and feedback degradation in Alternaria alternata.
    Article Snippet: Cell viability was assessed using propidium iodide (PI, Sigma-Aldrich) staining. .. Fluorescence was detected using a ZOE Fluorescent Cell Imager (Bio-Rad) with appropriate excitation and emission wavelengths, as previously described [34, 45]. ..

    Article Title: Dynamic Regulation of Atg4 Protease and Autophagy by Dithiothreitol and Iron in Alternaria alternata
    Article Snippet: .. Green fluorescence was observed using a ZOE Fluorescent Cell Imager (Bio-Rad) microscope equipped with a fluorescence filter set with excitation at 488 nm and emission at 510 nm. .. Vacuoles were stained with CMAC (7-amino-4-chloromethylcoumarin, 100 μM; Thermo Fisher Scientific, Waltham, MA, U.S.A.) and visualized with excitation at 353 nm and emission at 466 nm.

    Article Title: Grape Pomace Polyphenolic Extract Promotes Osteogenic Differentiation in Human Mesenchymal Stem Cells Through Activation of RUNX2 and NRF2 Transcription Factors: A Potential Natural Strategy for Osteoporosis Prevention.
    Article Snippet: .. Immune complexes were visualized with the ZOE Fluorescent Cell Imager (Bio-Rad Laboratories, Milan, Italy) inverted fluorescence system. https://doi.org/10.3390/biology15090719 .. Nuclear proteins were extracted from total cell lysates of MSCs induced to differentiate into osteoblasts using the Active Motif Nuclear Extract Kit (Active Motif, Carlsbad, CA, USA) according to the manufacturer’s protocol.

    Microscopy:

    Article Title: Dynamic Regulation of Atg4 Protease and Autophagy by Dithiothreitol and Iron in Alternaria alternata
    Article Snippet: .. Green fluorescence was observed using a ZOE Fluorescent Cell Imager (Bio-Rad) microscope equipped with a fluorescence filter set with excitation at 488 nm and emission at 510 nm. .. Vacuoles were stained with CMAC (7-amino-4-chloromethylcoumarin, 100 μM; Thermo Fisher Scientific, Waltham, MA, U.S.A.) and visualized with excitation at 353 nm and emission at 466 nm.

    Software:

    Article Title: Multi-omics analysis reveals integrin α3-dependent mechanisms of Zika virus oncolytic activity in pediatric neural tumors
    Article Snippet: Cells were seeded at 1×10 3 cells per well in 200 μL of medium in 96-well clear ultra-low attachment microplates (Thermo Fisher, cat. no. 10023683) to generate one tumorsphere per well. .. Images of the tumorspheres were taken daily using an Incucyte® S3 Live-Cell Analysis System (Sartorius, Göttingen, Germany) ( and ) and a ZOE Fluorescent Cell Imager (Bio Rad, Hercules, California, USA) ( and ; and ), and the area of the tumorspheres was measured using Image J software (version 1.54f; National Institutes of Health, USA; http://imagej.org ). ..



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    Long-term persistence of viable E. ruminantium within G. mellonella hemocytes. (A) Fluorescence microscopy of hemolymph collected 6 days post-infection, showing sustained intracellular bacterial presence within hemocytes. Nuclei are stained with Hoechst (blue) and bacteria with rhodamine (red). Scale bar, 30 μm. (B) Stereomicroscopy demonstrating whole-larva bacterial fluorescence persistence at 8 days post-infection. Scale bar, 5 mm. (C) Viability confirmation through re-infection assay. Hemolymph from infected G. mellonella was inoculated onto bovine aortic endothelial cell (BAEC) monolayers. At 4 days post-inoculation, characteristic morulae formation, lysis areas, and <t>fluorescent</t> bacteria within BAEC confirm maintenance of bacterial viability and infectivity throughout the larval infection period. Scale bar, 100 μm. N, nuclei; DPI, days post-infection.
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    Long-term persistence of viable E. ruminantium within G. mellonella hemocytes. (A) Fluorescence microscopy of hemolymph collected 6 days post-infection, showing sustained intracellular bacterial presence within hemocytes. Nuclei are stained with Hoechst (blue) and bacteria with rhodamine (red). Scale bar, 30 μm. (B) Stereomicroscopy demonstrating whole-larva bacterial fluorescence persistence at 8 days post-infection. Scale bar, 5 mm. (C) Viability confirmation through re-infection assay. Hemolymph from infected G. mellonella was inoculated onto bovine aortic endothelial cell (BAEC) monolayers. At 4 days post-inoculation, characteristic morulae formation, lysis areas, and fluorescent bacteria within BAEC confirm maintenance of bacterial viability and infectivity throughout the larval infection period. Scale bar, 100 μm. N, nuclei; DPI, days post-infection.

    Journal: bioRxiv

    Article Title: Galleria mellonella as a novel invertebrate model for studying Ehrlichia ruminantium pathogenesis and host-pathogen interactions

    doi: 10.64898/2026.04.29.721731

    Figure Lengend Snippet: Long-term persistence of viable E. ruminantium within G. mellonella hemocytes. (A) Fluorescence microscopy of hemolymph collected 6 days post-infection, showing sustained intracellular bacterial presence within hemocytes. Nuclei are stained with Hoechst (blue) and bacteria with rhodamine (red). Scale bar, 30 μm. (B) Stereomicroscopy demonstrating whole-larva bacterial fluorescence persistence at 8 days post-infection. Scale bar, 5 mm. (C) Viability confirmation through re-infection assay. Hemolymph from infected G. mellonella was inoculated onto bovine aortic endothelial cell (BAEC) monolayers. At 4 days post-inoculation, characteristic morulae formation, lysis areas, and fluorescent bacteria within BAEC confirm maintenance of bacterial viability and infectivity throughout the larval infection period. Scale bar, 100 μm. N, nuclei; DPI, days post-infection.

    Article Snippet: Samples were stained with 100 μL of 10 μg/mL Hoechst 33342 (Sigma-Aldrich) for 15-30 minutes at room temperature before microscopic examination using a fluorescent cell imager (ZOE, BioRad).

    Techniques: Fluorescence, Microscopy, Infection, Staining, Bacteria, Lysis