File:Actomyosin-dependent-dynamic-spatial-patterns-of-cytoskeletal-components-drive-mesoscale-podosome-ncomms13127-s12.ogv
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editDescriptionActomyosin-dependent-dynamic-spatial-patterns-of-cytoskeletal-components-drive-mesoscale-podosome-ncomms13127-s12.ogv |
English: Supplementary Movie 11 Lateral movement of a podosome cluster on a patterned surface. DCs were transfected with LifeAct-GFP and seeded on a scratched glass coverslip. Imaging was performed at a confocal microscope with 15 second frame intervals at 37°C and resulting time series were subjected to twSTICS analysis. The LifeAct-GFP Movie (right) is shown as a moving average of 10 frames to allow direct comparison with the vector maps (left), which are calculated over 10 frames. The arrows indicate direction of flow and the size and colour coding of the vectors are representative of the flow magnitude. Two cells are shown consecutively. Scale bar represents 10 μm. |
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Source | Video file from Meddens M, Pandzic E, Slotman J, Guillet D, Joosten B, Mennens S, Paardekooper L, Houtsmuller A, van den Dries K, Wiseman P, Cambi A (2016). "Actomyosin-dependent dynamic spatial patterns of cytoskeletal components drive mesoscale podosome organization". Nature Communications. DOI:10.1038/ncomms13127. PMID 27721497. PMC: 5062568. | ||
Author | Meddens M, Pandzic E, Slotman J, Guillet D, Joosten B, Mennens S, Paardekooper L, Houtsmuller A, van den Dries K, Wiseman P, Cambi A | ||
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This file is licensed under the Creative Commons Attribution 4.0 International license.
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current | 16:35, 29 October 2016 | 12 s, 1,049 × 411 (9.3 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 11 |
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Author | Meddens M, Pandzic E, Slotman J, Guillet D, Joosten B, Mennens S, Paardekooper L, Houtsmuller A, van den Dries K, Wiseman P, Cambi A |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Lateral movement of a podosome cluster on a patterned surface. DCs were transfected with LifeAct-GFP and seeded on a scratched glass coverslip. Imaging was performed at a confocal microscope with 15 second frame intervals at 37°C and resulting time series were subjected to twSTICS analysis. The LifeAct-GFP Movie (right) is shown as a moving average of 10 frames to allow direct comparison with the vector maps (left), which are calculated over 10 frames. The arrows indicate direction of flow and the size and colour coding of the vectors are representative of the flow magnitude. Two cells are shown consecutively. Scale bar represents 10 μm. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2016-10-10 |