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3d rendering analyses  (Oxford Instruments)


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    Structured Review

    Oxford Instruments 3d rendering analyses
    <t>3D</t> cell death analyses <t>of</t> <t>confocal</t> images of an I/R CS using Imaris software 3D rendering analyses of confocal images of an I/R CS stained with ethidium homodimer (yellow), and with antibodies against CD31 for endothelial cells (blue), cTNT for cardiomyocytes (red) and vimentim for fibroblasts (green). (A–D) (A) shows overlay of (B) highlighting all the dead cardiomyocytes, (C) highlighting dead endothelial cells and (D) highlighting dead fibroblasts, respectively. Scale Bar: 100 μM. Reused from ( <xref ref-type=Sharma et al., 2022 ). " width="250" height="auto" />
    3d Rendering Analyses, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44000 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/3d+rendering/Imaris/pmc09557725-486-16-14
    Average 99 stars, based on 44000 article reviews
    3d rendering analyses - by Bioz Stars, 2026-08
    99/100 stars

    Images

    1) Product Images from "In vitro modeling of myocardial ischemia/reperfusion injury with murine or human 3D cardiac spheroids"

    Article Title: In vitro modeling of myocardial ischemia/reperfusion injury with murine or human 3D cardiac spheroids

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2022.101751

    3D cell death analyses of confocal images of an I/R CS using Imaris software 3D rendering analyses of confocal images of an I/R CS stained with ethidium homodimer (yellow), and with antibodies against CD31 for endothelial cells (blue), cTNT for cardiomyocytes (red) and vimentim for fibroblasts (green). (A–D) (A) shows overlay of (B) highlighting all the dead cardiomyocytes, (C) highlighting dead endothelial cells and (D) highlighting dead fibroblasts, respectively. Scale Bar: 100 μM. Reused from ( <xref ref-type=Sharma et al., 2022 ). " title="3D cell death analyses of confocal images of an ..." property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: 3D cell death analyses of confocal images of an I/R CS using Imaris software 3D rendering analyses of confocal images of an I/R CS stained with ethidium homodimer (yellow), and with antibodies against CD31 for endothelial cells (blue), cTNT for cardiomyocytes (red) and vimentim for fibroblasts (green). (A–D) (A) shows overlay of (B) highlighting all the dead cardiomyocytes, (C) highlighting dead endothelial cells and (D) highlighting dead fibroblasts, respectively. Scale Bar: 100 μM. Reused from ( Sharma et al., 2022 ).

    Techniques Used: Software, Staining


    Figure Legend Snippet:

    Techniques Used: Isolation, Recombinant, Saline, Plasmid Preparation, Software, Microscopy, Imaging



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    Image Search Results


    Conversion of ND2 files to IMS files Double-click image to automatically convert files to.ims format for Imaris. ND2 files will have the white 3D box and right-pointing arrow icons in the lower left corner. IMS files will have the 3D box icon in the lower left corner.

    Journal: STAR Protocols

    Article Title: Protocol to study synapse density or volume—SynDOVE—in brain using confocal microscopy and Imaris three-dimensional surface rendering software

    doi: 10.1016/j.xpro.2026.104465

    Figure Lengend Snippet: Conversion of ND2 files to IMS files Double-click image to automatically convert files to.ims format for Imaris. ND2 files will have the white 3D box and right-pointing arrow icons in the lower left corner. IMS files will have the 3D box icon in the lower left corner.

    Article Snippet: • Below is a table ( ) that summarizes the recommended minimum image acquisition parameters for puncta detection and surface segmentation during 3D surface rendering in Imaris.

    Techniques: