File:Analysing-human-neural-stem-cell-ontogeny-by-consecutive-isolation-of-Notch-active-neural-ncomms7500-s7.ogv
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Analysing-human-neural-stem-cell-ontogeny-by-consecutive-isolation-of-Notch-active-neural-ncomms7500-s7.ogv (Ogg Theora video file, length 2.1 s, 512 × 512 pixels, 6.18 Mbps, file size: 1.57 MB)
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[edit]DescriptionAnalysing-human-neural-stem-cell-ontogeny-by-consecutive-isolation-of-Notch-active-neural-ncomms7500-s7.ogv |
English: Supplementary Movie 2 Three-dimensional reconstruction analysis of M-RG rosettes structure composition. Confocal z-sections of HES5::eGFP (green), combined with immunostaining for PAX6 (red) and DAPI staining for nuclei (blue) are shown. Image stacks with 17-19 planes per stack, at a spacing of 2 μm, and frame averaging of four images per plane were collected. All fluorescence images were confocal images of optical slice thickness ~0.9 μm. Scale bar: 50 μm. |
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Source | Video file from Edri R, Yaffe Y, Ziller M, Mutukula N, Volkman R, David E, Jacob-Hirsch J, Malcov H, Levy C, Rechavi G, Gat-Viks I, Meissner A, Elkabetz Y (2015). "Analysing human neural stem cell ontogeny by consecutive isolation of Notch active neural progenitors". Nature Communications. DOI:10.1038/ncomms7500. PMID 25799239. PMC: 4383005. | ||
Author | Edri R, Yaffe Y, Ziller M, Mutukula N, Volkman R, David E, Jacob-Hirsch J, Malcov H, Levy C, Rechavi G, Gat-Viks I, Meissner A, Elkabetz Y | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 15:36, 1 November 2016 | 2.1 s, 512 × 512 (1.57 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Short title | Supplementary Movie 2 |
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Author | Edri R, Yaffe Y, Ziller M, Mutukula N, Volkman R, David E, Jacob-Hirsch J, Malcov H, Levy C, Rechavi G, Gat-Viks I, Meissner A, Elkabetz Y |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Three-dimensional reconstruction analysis of M-RG rosettes structure composition. Confocal z-sections of HES5::eGFP (green), combined with immunostaining for PAX6 (red) and DAPI staining for nuclei (blue) are shown. Image stacks with 17-19 planes per stack, at a spacing of 2 μm, and frame averaging of four images per plane were collected. All fluorescence images were confocal images of optical slice thickness ~0.9 μm. Scale bar: 50 μm. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2015-03-23 |