3d (Oxford Instruments)
Oxford Instruments is a verified supplier 
Oxford Instruments manufactures this product 
99
Structured Review
Oxford Instruments
3d
3d, 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/3d+cell+tracking+algorithm/Imaris/pmc08714022-183-39-41
Average 99 stars, based on 44673 article reviews
3d, 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/3d+cell+tracking+algorithm/Imaris/pmc08714022-183-39-41
Average 99 stars, based on 44673 article reviews
3d - by Bioz Stars,
2026-11
99/100 stars
Images
1) Product Images from "Microglia in the developing retina couple phagocytosis with the progression of apoptosis via P2RY12 signaling"
Article Title: Microglia in the developing retina couple phagocytosis with the progression of apoptosis via P2RY12 signaling
Journal: Developmental dynamics : an official publication of the American Association of Anatomists
doi: 10.1002/dvdy.163
Figure Legend Snippet: A-D. Each circle is color coded for each embryo imaged, and overlaid onto box plots. A. Total number of AO+ cells observed during live imaging from ~54-62 hours post fertilization (hpf). B. The percent of AO+ cells that were observed to be engulfed by a microglial cell during the imaging session. C. For AO+ cells observed to be cleared by microglia, the percent showing association with a microglial cell at the onset of AO+ signal. D. Each circle represents individual cells from each embryo that was imaged. A selected number of individual AO+ cells, which were observed to appear and be cleared, during the imaging session were tracked in each embryo imaged. The duration of AO signal is shown for these individual AO+ cells. E-F represent max projections of selected, flattened z planes over a selected time-lapse. E. Shows the initial detection of an AO+ cell (green, indicated by red-orange arrow) associated with a microglial cell (microglia=magenta). E’. Shows the same AO+ cell (green, indicated by the magenta arrow) 80 minutes later, just before the AO signal is lost, after it had moved with the migrating microglial cell (magenta). F. The movement of the AO+ cell body was temporally color-coded to show its dynamic movement over time; the AO+ cell was associated with a microglial cell at all time frames. The color scale on the right indicates progression of time, where the first frame corresponds to 0:00 and the last frame is 85:00 (min:sec). Scale bar in bottom right of F = 5 microns and applies to E-F. G and H. To show a representation of dynamics of AO+ cell movement in association with microglia, a subset of AO+ cells were tracked in 3D using Imaris software. Quantifications show the speed (G) and total displacement (H) of individual AO+ cell bodies. Box plots are shown and circles are color coded to represent each embryo imaged. Each circle represents one AO+ cell that was tracked in each embryo that was imaged. Results are shown for n=6 different embryos.
Techniques Used: Imaging, Software
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 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 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 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 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 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 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. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using 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 Cytometry: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 Flow Cytometry: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 Structured Illumination 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 Micro-CT: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 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. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using Mouse 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. For 3D reconstruction and morphological analysis of oligodendrocytes in line CNPMTO- C, z- stacks were acquired at 0.5 μm intervals and processed using 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 |