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3d visualization program 'weblab viewerpro, version 3.20  (Molecular Simulations Inc)

 
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    Molecular Simulations Inc 3d visualization program 'weblab viewerpro, version 3.20
    3d Visualization Program 'Weblab Viewerpro, Version 3.20, supplied by Molecular Simulations Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/3d+immersive+visualization+program/3d+visualization+program++weblab+viewerpro++version+3+20/pm12383264-111-29-36
    Average 90 stars, based on 1 article reviews
    3d visualization program 'weblab viewerpro, version 3.20 - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Comparison:

    Article Title: Purification, crystallization, NMR spectroscopy and biochemical analyses of alpha-phycoerythrocyanin peptides.
    Article Snippet: All sequences were determined with an Applied Biosystems sequencer model 473 A following the manufacturer’s instructions. .. Structural comparison of the intact a-PEC and the degraded a-PEC peptide 2 The picture comparing the secondary structures of the intact subunit and peptide 2 was produced with the 3D visualization program ‘WebLab ViewerPro, Version 3.20’ (Molecular Simulations Inc.). ..

    Produced:

    Article Title: Purification, crystallization, NMR spectroscopy and biochemical analyses of alpha-phycoerythrocyanin peptides.
    Article Snippet: All sequences were determined with an Applied Biosystems sequencer model 473 A following the manufacturer’s instructions. .. Structural comparison of the intact a-PEC and the degraded a-PEC peptide 2 The picture comparing the secondary structures of the intact subunit and peptide 2 was produced with the 3D visualization program ‘WebLab ViewerPro, Version 3.20’ (Molecular Simulations Inc.). ..



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    Experimental design for cell counting using <t>3D</t> virtual reality. (A) Serial sections containing MNTB from Cre;Ai9 mice were stained with cell-specific antibodies for neurons (Map2), astrocytes (Aldh1L1), oligodendrocytes (Sox10) and microglia (Iba1), in an alternating manner, along with DAPI. These slices were imaged with a 40× objective and tiled. The MNTB is outlined in white in each section and the midline is indicated by a dashed white line. Scale bar = 100 μm. (B) The MNTB was cropped from the larger image and imported <t>into</t> <t>syGlass</t> for cell counting in 3D virtual reality. The solid and dashed white lines demarcate cut planes that were rotated to generate the 3D view in C (arrow). Scale bar = 50 μm. (C) Rotated view of part of MNTB to illustrate 3D view for cell counting. Counting dots were placed onto the nuclei. White dots indicate incomplete (sectioned) nuclei in the first slice of the z-stack. These were excluded from analysis, but incomplete nuclei in the bottom slice were counted and included in the analysis. Red dots indicate cells that were counted. Note that cells throughout the entire MNTB (panel B) were counted.
    3d Immersive Visualization Program, supplied by syGlass Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/3d+immersive+visualization+program/virtual+reality+software/pmc09245928-234-2-1
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    Image Search Results


    Experimental design for cell counting using 3D virtual reality. (A) Serial sections containing MNTB from Cre;Ai9 mice were stained with cell-specific antibodies for neurons (Map2), astrocytes (Aldh1L1), oligodendrocytes (Sox10) and microglia (Iba1), in an alternating manner, along with DAPI. These slices were imaged with a 40× objective and tiled. The MNTB is outlined in white in each section and the midline is indicated by a dashed white line. Scale bar = 100 μm. (B) The MNTB was cropped from the larger image and imported into syGlass for cell counting in 3D virtual reality. The solid and dashed white lines demarcate cut planes that were rotated to generate the 3D view in C (arrow). Scale bar = 50 μm. (C) Rotated view of part of MNTB to illustrate 3D view for cell counting. Counting dots were placed onto the nuclei. White dots indicate incomplete (sectioned) nuclei in the first slice of the z-stack. These were excluded from analysis, but incomplete nuclei in the bottom slice were counted and included in the analysis. Red dots indicate cells that were counted. Note that cells throughout the entire MNTB (panel B) were counted.

    Journal: Developmental neurobiology

    Article Title: Glial Cell Expansion Coincides with Neural Circuit Formation in the Developing Auditory Brainstem

    doi: 10.1002/dneu.22633

    Figure Lengend Snippet: Experimental design for cell counting using 3D virtual reality. (A) Serial sections containing MNTB from Cre;Ai9 mice were stained with cell-specific antibodies for neurons (Map2), astrocytes (Aldh1L1), oligodendrocytes (Sox10) and microglia (Iba1), in an alternating manner, along with DAPI. These slices were imaged with a 40× objective and tiled. The MNTB is outlined in white in each section and the midline is indicated by a dashed white line. Scale bar = 100 μm. (B) The MNTB was cropped from the larger image and imported into syGlass for cell counting in 3D virtual reality. The solid and dashed white lines demarcate cut planes that were rotated to generate the 3D view in C (arrow). Scale bar = 50 μm. (C) Rotated view of part of MNTB to illustrate 3D view for cell counting. Counting dots were placed onto the nuclei. White dots indicate incomplete (sectioned) nuclei in the first slice of the z-stack. These were excluded from analysis, but incomplete nuclei in the bottom slice were counted and included in the analysis. Red dots indicate cells that were counted. Note that cells throughout the entire MNTB (panel B) were counted.

    Article Snippet: The syGlass 3D immersive visualization program was used to perform cell counts because it enables rapid and accurate assessment of sectioned DAPI-labeled nuclei at the edge of the first image plane , and it permits accurate assessment of spatial association of markers with DAPI in three dimensions.

    Techniques: Cell Counting, Staining