File:Microtubules-Depolymerization-Caused-by-the-CK1-Inhibitor-IC261-May-Be-Not-Mediated-by-CK1-Blockage-pone.0100090.s009.ogv
Microtubules-Depolymerization-Caused-by-the-CK1-Inhibitor-IC261-May-Be-Not-Mediated-by-CK1-Blockage-pone.0100090.s009.ogv (Ogg Theora video file, length 24 s, 302 × 227 pixels, 3.35 Mbps, file size: 9.64 MB)
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[edit]DescriptionMicrotubules-Depolymerization-Caused-by-the-CK1-Inhibitor-IC261-May-Be-Not-Mediated-by-CK1-Blockage-pone.0100090.s009.ogv |
English: Microtubule depolymerization by IC261 treatment is reversible. CV-1 cells expressing EYFP-tubulin were treated at time point “0 min” with 3.2 µM IC261 and observed by time-resolved fluorescence microscopy. The spindle apparatus of the exemplary cell shown here was dissolved within 8 min. At time point “10 min” IC261 was removed by exchange of media. Within a few minutes spindle MTs were built up again (“15 min”) and 20 min after removal a morphologically unimpaired spindle apparatus had been developed (“30 min”). After 2 h the cell proceeded into anaphase and cytokinesis (“155 min”). |
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Source | Movie S5 from Stoter M, Kruger M, Banting G, Henne-Bruns D, Knippschild U (2014). "Microtubules Depolymerization Caused by the CK1 Inhibitor IC261 May Be Not Mediated by CK1 Blockage". PLOS ONE. DOI:10.1371/journal.pone.0100090. PMID 24937750. PMC: 4061085. | ||
Author | Stoter M, Kruger M, Banting G, Henne-Bruns D, Knippschild U | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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current | 21:57, 11 July 2014 | 24 s, 302 × 227 (9.64 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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Author | Stoter M, Kruger M, Banting G, Henne-Bruns D, Knippschild U |
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Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Microtubule depolymerization by IC261 treatment is reversible. CV-1 cells expressing EYFP-tubulin were treated at time point “0 min” with 3.2 µM IC261 and observed by time-resolved fluorescence microscopy. The spindle apparatus of the exemplary cell shown here was dissolved within 8 min. At time point “10 min” IC261 was removed by exchange of media. Within a few minutes spindle MTs were built up again (“15 min”) and 20 min after removal a morphologically unimpaired spindle apparatus had been developed (“30 min”). After 2 h the cell proceeded into anaphase and cytokinesis (“155 min”). |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2014 |