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deconvolution module clearview 9 5  (Oxford Instruments)


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    Structured Review

    Oxford Instruments deconvolution module clearview 9 5
    Deconvolution Module Clearview 9 5, 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/deconvolution+module/Imaris/pmc12780313-60-6-5
    Average 99 stars, based on 44673 article reviews
    deconvolution module clearview 9 5 - 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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    Image Search Results


    ( A , B ) HUVEC were treated with histamine (100 µM, Sigma-Aldrich) or thrombin (1 U/ml, CalBiochem) for 10 min, or left untreated with equivalent volumes of vehicle (media) as controls. Cells were subsequently fixed, permeabilized and stained for plakoglobin, β-catenin, and VE-cadherin, all visualized in grayscale to ensure unbiased comparative analysis. Higher magnification images (63X) were acquired using a Zeiss LSM 980 confocal microscope equipped with an Airyscan detector ( A ), while lower magnification images (40X) were captured on a Zeiss LSM 880 confocal microscope ( B ). Scale bars, 25 µm.

    Journal: The EMBO Journal

    Article Title: Plakoglobin transmits tension across VE-cadherin for vascular leak formation and leukocyte diapedesis

    doi: 10.1038/s44318-026-00732-0

    Figure Lengend Snippet: ( A , B ) HUVEC were treated with histamine (100 µM, Sigma-Aldrich) or thrombin (1 U/ml, CalBiochem) for 10 min, or left untreated with equivalent volumes of vehicle (media) as controls. Cells were subsequently fixed, permeabilized and stained for plakoglobin, β-catenin, and VE-cadherin, all visualized in grayscale to ensure unbiased comparative analysis. Higher magnification images (63X) were acquired using a Zeiss LSM 980 confocal microscope equipped with an Airyscan detector ( A ), while lower magnification images (40X) were captured on a Zeiss LSM 880 confocal microscope ( B ). Scale bars, 25 µm.

    Article Snippet: Zeiss LSM 980 Airyscan acquisitions were processed with Airyscan Joint Deconvolution processing module in ZEN blue software (Zeiss) to improve signal-to-noise and spatial resolution; LSM 880 images were used without further deconvolution.

    Techniques: Staining, Microscopy