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time lapse live cell microscopy  (Carl Zeiss)


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    Carl Zeiss time lapse live cell microscopy
    Time Lapse Live Cell Microscopy, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 98/100, based on 982 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/time+lapse+live+cell+microscopy/Inverted+microscope+Axio+Observer+7/bio_rxiv__64898__2025__12__22__695944-58-5-11
    Average 98 stars, based on 982 article reviews
    time lapse live cell microscopy - by Bioz Stars, 2026-09
    98/100 stars

    Images

    Related Articles

    Migration:

    Article Title: Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels
    Article Snippet: .. Cell migration was monitored using time-lapse live-cell microscopy (Axio Observer 7, Zeiss, Germany; Eclipse Ti-E inverted microscope, Nikon, The Netherlands). ..

    Microscopy:

    Article Title: Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels
    Article Snippet: .. Cell migration was monitored using time-lapse live-cell microscopy (Axio Observer 7, Zeiss, Germany; Eclipse Ti-E inverted microscope, Nikon, The Netherlands). ..

    Inverted Microscopy:

    Article Title: Discrete viscoelastic model of deformable immune cell migration through confined tumor microchannels
    Article Snippet: .. Cell migration was monitored using time-lapse live-cell microscopy (Axio Observer 7, Zeiss, Germany; Eclipse Ti-E inverted microscope, Nikon, The Netherlands). ..



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    Image Search Results


    (A) The platemap showing replicates of ten different doses of staurosporine, an apoptosis-inducing compound. We imaged each well at four fields of view (FOVs) at three z slices, each 3um apart. Images were acquired every 30 minutes for 360 minutes (six hours), capturing Hoechst, ChromaLIVE 488_yellow, ChromaLIVE 488_red, and ChromaLIVE 561. We fixed cells at six hours and stained for AnnexinV, an apoptotic marker, and Hoechst. (B) Our HCLTI pipeline for processing time-lapse microscopy images. (C) Representative images of tracked HeLa single cells across time for varying doses of staurosporine. Cyan represents nuclei, yellow represents ChromaLive 561, and Magenta represents ChromaLive 488 at both its emission channels for visualization purposes only. Scale bars = 10 um.

    Journal: bioRxiv

    Article Title: High-content live-cell time-lapse imaging predicts cells about to die via apoptosis

    doi: 10.1101/2025.10.23.684203

    Figure Lengend Snippet: (A) The platemap showing replicates of ten different doses of staurosporine, an apoptosis-inducing compound. We imaged each well at four fields of view (FOVs) at three z slices, each 3um apart. Images were acquired every 30 minutes for 360 minutes (six hours), capturing Hoechst, ChromaLIVE 488_yellow, ChromaLIVE 488_red, and ChromaLIVE 561. We fixed cells at six hours and stained for AnnexinV, an apoptotic marker, and Hoechst. (B) Our HCLTI pipeline for processing time-lapse microscopy images. (C) Representative images of tracked HeLa single cells across time for varying doses of staurosporine. Cyan represents nuclei, yellow represents ChromaLive 561, and Magenta represents ChromaLive 488 at both its emission channels for visualization purposes only. Scale bars = 10 um.

    Article Snippet: – We then applied the Live Cell Painting assay (ChromaLIVE TM ) , and performed live-cell time-lapse spinning disk confocal microscopy (Yokogawa CQ1), acquiring images per field of view (FOV) every 30 minutes in three z stacks for six hours.

    Techniques: Staining, Marker, Time-lapse Microscopy

    Journal: bioRxiv

    Article Title: High-content live-cell time-lapse imaging predicts cells about to die via apoptosis

    doi: 10.1101/2025.10.23.684203

    Figure Lengend Snippet:

    Article Snippet: – We then applied the Live Cell Painting assay (ChromaLIVE TM ) , and performed live-cell time-lapse spinning disk confocal microscopy (Yokogawa CQ1), acquiring images per field of view (FOV) every 30 minutes in three z stacks for six hours.

    Techniques: Imaging, Staining