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mct volume realistic 3d visualization software (SCANCO USA INC)

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SCANCO USA INC mct volume realistic 3d visualization software
Mct Volume Realistic 3d Visualization Software, supplied by SCANCO USA 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/l+ct+volume+realistic+3d+visualization+software+from+mct+evaluation+program++scanco+m+ct++v+6+5+1++switzerland+/pm30208806-75-1-11
Average 90 stars, based on 1 article reviews

mct volume realistic 3d visualization software - by Bioz Stars, 2026-10

90/100 stars

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Article Title: Osteoinduction of stem cells by collagen peptide-immobilized hydrolyzed poly(butylene succinate)/β-tricalcium phosphate scaffold for bone tissue engineering.
Article Snippet: Bone substitute is a therapeutic approach to treat bone abnormalities.. A scaffold serves mainly as osteoconductive elements.. To facilitate a better biological performance, short collagen peptide was immobilized onto hydrolyzed poly(butylene succinate)/b-tricalcium phosphate (HPBSu/TCP) scaffolds.

Article Title: PCL/PHBV blended three dimensional scaffolds fabricated by fused deposition modeling and responses of chondrocytes to the scaffolds.
Article Snippet: In this study, poly(e-caprolactone)/poly(3-hydroxybutyrate-co23-hydroxyvalerate) (PCL/PHBV) blended porous scaffolds were fabricated by fused deposition modeling (FDM).. PCL/PHBV filaments, initially prepared at different weight ratios, that is, 100/0, 75/25, 50/50, and 25/75, were fabricated by the lay-down pattern of 0/90/45/1358 to obtain scaffolds with dimension of 6.0 3 6.0 3 2.5 mm and average filament diameters and channel sizes in the ranges of 370– 390 mm and 190–210 mm, respectively.. To enhance the surface hydrophilicity of the materials, the scaffolds were subsequently subjected to a low pressure oxygen plasma treatment.

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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