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hcs studio 2 0 morphology explorer bioapplication module  (Thermo Fisher)


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    Structured Review

    Thermo Fisher hcs studio 2 0 morphology explorer bioapplication module
    Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.
    Hcs Studio 2 0 Morphology Explorer Bioapplication Module, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hcs+studio+2+0+morphology+explorer+bioapplication+module/pmc06074874-462-13-20
    Average 86 stars, based on 1 article reviews
    hcs studio 2 0 morphology explorer bioapplication module - by Bioz Stars, 2026-09
    86/100 stars

    Images

    1) Product Images from "From the Cover: An Animal-Free In Vitro Three-Dimensional Testicular Cell Coculture Model for Evaluating Male Reproductive Toxicants"

    Article Title: From the Cover: An Animal-Free In Vitro Three-Dimensional Testicular Cell Coculture Model for Evaluating Male Reproductive Toxicants

    Journal: Toxicological Sciences

    doi: 10.1093/toxsci/kfx139

    Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.
    Figure Legend Snippet: Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.

    Techniques Used: Labeling

    Related Articles

    Labeling:

    Article Title: From the Cover: An Animal-Free In Vitro Three-Dimensional Testicular Cell Coculture Model for Evaluating Male Reproductive Toxicants
    Article Snippet: The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts).



    Similar Products

    hcs studio 2 0 morphology explorer bioapplication module  (Thermo Fisher)
    86
    Thermo Fisher hcs studio 2 0 morphology explorer bioapplication module
    Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.
    Hcs Studio 2 0 Morphology Explorer Bioapplication Module, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hcs+studio+2+0+morphology+explorer+bioapplication+module/pmc06074874-462-13-20
    Average 86 stars, based on 1 article reviews
    hcs studio 2 0 morphology explorer bioapplication module - by Bioz Stars, 2026-09
    86/100 stars
    		  Buy from Supplier

    Image Search Results


    Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.

    Journal: Toxicological Sciences

    Article Title: From the Cover: An Animal-Free In Vitro Three-Dimensional Testicular Cell Coculture Model for Evaluating Male Reproductive Toxicants

    doi: 10.1093/toxsci/kfx139

    Figure Lengend Snippet: Single-cell-based quantification of F-actin cytoskeletal structure. The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts). Cytoskeletal rearrangement analysis was conducted in the images obtained from the coculture model (A), and automatic segmentation of the nuclei images cells (blue line, B) and cellular outline (yellow line, C) were conducted. The localization and orientation of F-actin fibers were determined (C, green). A statistical summary of F-actin fibers was identified from bar charts and scatter plots (D). Actin fibers greater than a threshold length were identified and labeled with green, and the fiber intensity over 100 pixels were highlighted with red overlay (D), indicating F-actin bundle formation across cells in the coculture model.

    Article Snippet: The multi-channel images were automatically captured using an Arrayscan VTI HCS reader with HCS Studio 2.0 Morphology Explorer BioApplication module (Thermo Fisher Scientific, Massachusetts).

    Techniques: Labeling