File:Fluorescent-Protein-Stabilization-and-High-Resolution-Imaging-of-Cleared-Intact-Mouse-Brains-pone.0124650.s010.ogv

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Original file (Ogg Theora video file, length 2 min 0 s, 1,024 × 768 pixels, 1.1 Mbps, file size: 15.8 MB)

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English: Video animation of RABV ΔG-EGFP (EnvA) infected neurons in EC showing axon traces of monosynaptically connected neurons. Right hemisphere horizontal dataset (same as shown in Fig 4) was downsampled to 6.45 μm cubic voxel size and converted from 16 bit greyscale TIFF into 8 bit Amira Mesh format. Four 3D traces of axons manually generated with KNOSSOS software were overlaid as color-coded, solid lines with the EGFP channel (color-coded grey) for generating part of the animation. The trajectory of one of the axons traced with KNOSSOS is depicted by a series of red dots after zooming in to the original 1.61 x 1.61 μm xy pixel size. Note the autofluorescence of the brain periphery.
Date
Source S6 Video from Schwarz M, Scherbarth A, Sprengel R, Engelhardt J, Theer P, Giese G (2015). "Fluorescent-Protein Stabilization and High-Resolution Imaging of Cleared, Intact Mouse Brains". PLOS ONE. DOI:10.1371/journal.pone.0124650. PMID 25993380. PMC: 4439039.
Author Schwarz M, Scherbarth A, Sprengel R, Engelhardt J, Theer P, Giese G
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Date/TimeThumbnailDimensionsUserComment
current20:35, 31 May 20152 min 0 s, 1,024 × 768 (15.8 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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Format Bitrate Download Status Encode time
VP9 720P 429 kbps Completed 00:04, 27 August 2018 2 min 58 s
VP9 480P 199 kbps Completed 00:02, 27 August 2018 1 min 35 s
VP9 360P 101 kbps Completed 00:02, 27 August 2018 1 min 10 s
VP9 240P 53 kbps Completed 00:01, 27 August 2018 58 s
WebM 360P 487 kbps Completed 06:28, 20 November 2016 18 min 22 s
QuickTime 144p (MJPEG) 563 kbps Completed 20:37, 25 October 2024 4.0 s

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