File:Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv002.ogv
No higher resolution available.
Dual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv002.ogv (Ogg Theora video file, length 14 s, 552 × 277 pixels, 277 kbps, file size: 469 KB)
File information
Structured data
Captions
Summary edit
DescriptionDual-Role-of-Topoisomerase-II-in-Centromere-Resolution-and-Aurora-B-Activity-pbio.0060207.sv002.ogv |
English: Time-Lapse Microscopy of S2 Cells Stably Expressing CID-GFP and RFP-H2B and Depleted for TOPO II, 72 h after the Addition of the dsRNA Z-stacks are composed of ten optical sections covering 10 μm and were acquired every 20 s. Each Z-stack is 10 μm and composed of ten optical sections. Anaphase onset corresponds to time 0 s. Merge color images of RFP-H2B (red) and CID-GFP (green) channels are shown on the left. The CID-GFP (white) channel is shown alone on the right. The two CID-GFP pairs of each centromere were identified and labeled in every layer composing the Z-stacks at the different time points. The mean distance between CID-GFP dots is approximately 1 μm. Tracking of kinetochore pairs was performed using a plug-in for the Image J software. In the video, each CID-GFP pair is labeled with the same color. |
||
Date | |||
Source | Video S2 from Coelho P, Queiroz-Machado J, Carmo A, Moutinho-Pereira S, Maiato H, Sunkel C (2008). "Dual Role of Topoisomerase II in Centromere Resolution and Aurora B Activity". PLOS Biology. DOI:10.1371/journal.pbio.0060207. PMID 18752348. PMC: 2525683. | ||
Author | Coelho P, Queiroz-Machado J, Carmo A, Moutinho-Pereira S, Maiato H, Sunkel C | ||
Permission (Reusing this file) |
|
||
Provenance InfoField |
|
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 23:24, 30 October 2012 | 14 s, 552 × 277 (469 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
You cannot overwrite this file.
File usage on Commons
There are no pages that use this file.
Transcode status
Update transcode statusMetadata
This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. The timestamp is only as accurate as the clock in the camera, and it may be completely wrong.
Short title | Time-Lapse Microscopy of S2 Cells Stably Expressing CID-GFP and RFP-H2B and Depleted for TOPO II, 72 h after the Addition of the dsRNA |
---|---|
Author | Coelho P, Queiroz-Machado J, Carmo A, Moutinho-Pereira S, Maiato H, Sunkel C |
Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Z-stacks are composed of ten optical sections covering 10 ?m and were acquired every 20 s. Each Z-stack is 10 ?m and composed of ten optical sections. Anaphase onset corresponds to time 0 s. Merge color images of RFP-H2B (red) and CID-GFP (green) channels are shown on the left. The CID-GFP (white) channel is shown alone on the right. The two CID-GFP pairs of each centromere were identified and labeled in every layer composing the Z-stacks at the different time points. The mean distance between CID-GFP dots is approximately 1 ?m. Tracking of kinetochore pairs was performed using a plug-in for the Image J software. In the video, each CID-GFP pair is labeled with the same color. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2008-08 |