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imaris 3 d image software  (Oxford Instruments)


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    Structured Review

    Oxford Instruments imaris 3 d image software
    (A, <t>B)</t> <t>3-D</t> Imaris confocal images of VG from E13 normal chick ( ; 1-Normal). (A) Semitransparent colors were used to define the medulla oblongata (aqua), vestibular nerve (pink) between VG and medulla oblongata, vestibular ganglion (pink line outlines VG with neurons labeled with yellow dots), lateral vestibular nerve (green) and posterior vestibular nerve (purple). The anterior vestibular nerve is not shown. (B) Dorsal surface of image in A has been tilted downward so that 20 μm sections containing the counted neurons appear as stripes separated by 60 μm uncounted neuron intervals.
    Imaris 3 D Image Software, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44474 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/imaris+3+d+image+software/Imaris/pmc12947391-106-19-25
    Average 99 stars, based on 44474 article reviews
    imaris 3 d image software - by Bioz Stars, 2026-11
    99/100 stars

    Images

    1) Product Images from "Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders"

    Article Title: Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders

    Journal: Frontiers in Neurology

    doi: 10.3389/fneur.2026.1721001

    (A, B) 3-D Imaris confocal images of VG from E13 normal chick ( ; 1-Normal). (A) Semitransparent colors were used to define the medulla oblongata (aqua), vestibular nerve (pink) between VG and medulla oblongata, vestibular ganglion (pink line outlines VG with neurons labeled with yellow dots), lateral vestibular nerve (green) and posterior vestibular nerve (purple). The anterior vestibular nerve is not shown. (B) Dorsal surface of image in A has been tilted downward so that 20 μm sections containing the counted neurons appear as stripes separated by 60 μm uncounted neuron intervals.
    Figure Legend Snippet: (A, B) 3-D Imaris confocal images of VG from E13 normal chick ( ; 1-Normal). (A) Semitransparent colors were used to define the medulla oblongata (aqua), vestibular nerve (pink) between VG and medulla oblongata, vestibular ganglion (pink line outlines VG with neurons labeled with yellow dots), lateral vestibular nerve (green) and posterior vestibular nerve (purple). The anterior vestibular nerve is not shown. (B) Dorsal surface of image in A has been tilted downward so that 20 μm sections containing the counted neurons appear as stripes separated by 60 μm uncounted neuron intervals.

    Techniques Used: Labeling

    Confocal images of VG analyzed with Imaris from normal chick in horizontal sections with dorsal plane on the image surface (directional arrows in A; A-C; 1-Normal). The images are more tilted in the dorsoventral axis compared to . (A) 3-D Imaris image. (B) Higher magnification image of VG neurons in A. (C) Higher magnification images of VG neurons in (B) to show the consolidated mass of VG neurons characteristic of E13 normal chicks.
    Figure Legend Snippet: Confocal images of VG analyzed with Imaris from normal chick in horizontal sections with dorsal plane on the image surface (directional arrows in A; A-C; 1-Normal). The images are more tilted in the dorsoventral axis compared to . (A) 3-D Imaris image. (B) Higher magnification image of VG neurons in A. (C) Higher magnification images of VG neurons in (B) to show the consolidated mass of VG neurons characteristic of E13 normal chicks.

    Techniques Used:

    3-D Imaris image from rotated side of ARO chick. TN is labeled on its anterior surface. Series of arrows demarcate the lateral brain surface. (B) Higher magnification image of VG neurons in (A) . (C) Higher magnification image of VG neurons in B to show segregated VG neuron cell bodies on rotated side of ARO chick rather than a consolidated mass found in normal E13 chicks (see Figure 5 ).
    Figure Legend Snippet: 3-D Imaris image from rotated side of ARO chick. TN is labeled on its anterior surface. Series of arrows demarcate the lateral brain surface. (B) Higher magnification image of VG neurons in (A) . (C) Higher magnification image of VG neurons in B to show segregated VG neuron cell bodies on rotated side of ARO chick rather than a consolidated mass found in normal E13 chicks (see Figure 5 ).

    Techniques Used: Labeling

    Related Articles

    Software:

    Article Title: Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders
    Article Snippet: .. The number of VG neurons in E13 normal and ARO chicks was estimated from 3-D serial confocal images using Imaris 3-D image software (version 9.8.0; Bitplane AG). ..



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    Image Search Results


    (A, B) 3-D Imaris confocal images of VG from E13 normal chick ( ; 1-Normal). (A) Semitransparent colors were used to define the medulla oblongata (aqua), vestibular nerve (pink) between VG and medulla oblongata, vestibular ganglion (pink line outlines VG with neurons labeled with yellow dots), lateral vestibular nerve (green) and posterior vestibular nerve (purple). The anterior vestibular nerve is not shown. (B) Dorsal surface of image in A has been tilted downward so that 20 μm sections containing the counted neurons appear as stripes separated by 60 μm uncounted neuron intervals.

    Journal: Frontiers in Neurology

    Article Title: Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders

    doi: 10.3389/fneur.2026.1721001

    Figure Lengend Snippet: (A, B) 3-D Imaris confocal images of VG from E13 normal chick ( ; 1-Normal). (A) Semitransparent colors were used to define the medulla oblongata (aqua), vestibular nerve (pink) between VG and medulla oblongata, vestibular ganglion (pink line outlines VG with neurons labeled with yellow dots), lateral vestibular nerve (green) and posterior vestibular nerve (purple). The anterior vestibular nerve is not shown. (B) Dorsal surface of image in A has been tilted downward so that 20 μm sections containing the counted neurons appear as stripes separated by 60 μm uncounted neuron intervals.

    Article Snippet: The number of VG neurons in E13 normal and ARO chicks was estimated from 3-D serial confocal images using Imaris 3-D image software (version 9.8.0; Bitplane AG).

    Techniques: Labeling

    Confocal images of VG analyzed with Imaris from normal chick in horizontal sections with dorsal plane on the image surface (directional arrows in A; A-C; 1-Normal). The images are more tilted in the dorsoventral axis compared to . (A) 3-D Imaris image. (B) Higher magnification image of VG neurons in A. (C) Higher magnification images of VG neurons in (B) to show the consolidated mass of VG neurons characteristic of E13 normal chicks.

    Journal: Frontiers in Neurology

    Article Title: Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders

    doi: 10.3389/fneur.2026.1721001

    Figure Lengend Snippet: Confocal images of VG analyzed with Imaris from normal chick in horizontal sections with dorsal plane on the image surface (directional arrows in A; A-C; 1-Normal). The images are more tilted in the dorsoventral axis compared to . (A) 3-D Imaris image. (B) Higher magnification image of VG neurons in A. (C) Higher magnification images of VG neurons in (B) to show the consolidated mass of VG neurons characteristic of E13 normal chicks.

    Article Snippet: The number of VG neurons in E13 normal and ARO chicks was estimated from 3-D serial confocal images using Imaris 3-D image software (version 9.8.0; Bitplane AG).

    Techniques:

    3-D Imaris image from rotated side of ARO chick. TN is labeled on its anterior surface. Series of arrows demarcate the lateral brain surface. (B) Higher magnification image of VG neurons in (A) . (C) Higher magnification image of VG neurons in B to show segregated VG neuron cell bodies on rotated side of ARO chick rather than a consolidated mass found in normal E13 chicks (see Figure 5 ).

    Journal: Frontiers in Neurology

    Article Title: Loss of embryonic vestibular ganglion neurons in a chick model of congenital vestibular disorders

    doi: 10.3389/fneur.2026.1721001

    Figure Lengend Snippet: 3-D Imaris image from rotated side of ARO chick. TN is labeled on its anterior surface. Series of arrows demarcate the lateral brain surface. (B) Higher magnification image of VG neurons in (A) . (C) Higher magnification image of VG neurons in B to show segregated VG neuron cell bodies on rotated side of ARO chick rather than a consolidated mass found in normal E13 chicks (see Figure 5 ).

    Article Snippet: The number of VG neurons in E13 normal and ARO chicks was estimated from 3-D serial confocal images using Imaris 3-D image software (version 9.8.0; Bitplane AG).

    Techniques: Labeling