standard image processing software (Oxford Instruments)
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Oxford Instruments
standard image processing software
Standard Image Processing 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/cellsens+imaging+software+program/Imaris/us09122951-15-8-24
Average 99 stars, based on 44474 article reviews
Standard Image Processing 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/cellsens+imaging+software+program/Imaris/us09122951-15-8-24
Average 99 stars, based on 44474 article reviews
standard image processing software - by Bioz Stars,
2026-11
99/100 stars
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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 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 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 Western Blot: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 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 Drosophila: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 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 Blocking Assay:Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines. Article Snippet: adjusted for brightness and contrast with Fiji. 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For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Quantitative RT-PCR: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 Gene Expression: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 Expressing: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 Confocal Laser Scanning 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 Next-Generation Sequencing:Article Title: Red Fluorescent Labeling of Myelin by Membrane-Targeted tdTomato in Transgenic Mouse Lines. Article Snippet: adjusted for brightness and contrast with Fiji. 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