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autoaligner alignment software  (Oxford Instruments)


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  • 99

    Structured Review

    Oxford Instruments autoaligner alignment software
    Autoaligner Alignment Software, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44673 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/Alignment+Software/Imaris/pmc13627376-70-12-15
    Average 99 stars, based on 44673 article reviews
    autoaligner alignment software - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Analysis:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Generated:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Confocal:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Staining:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Microscopy:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Fluorescence:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Software:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Imaging:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Plasmid Preparation:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Suspension:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    In Vitro:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Incubation:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Lysis:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Gentle:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Morphology:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Tissue:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Z-Stacks:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide

    Fluorescence Microscopy:

    Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines.
    Article Snippet: adjusted for brightness and contrast with Fiji. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Imaris (version 10.2) for 3D reconstruction (Surface mode) and myelin sheath measurements (Filament mode). Optic and sciatic nerves were whole- mounted (Fluoromount- G, Invitrogen) on SuperFrost slide



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