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File:Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S5.ogv

Trapping-of-normal-EB1-ligands-in-aggresomes-formed-by-an-EB1-deletion-mutant-1471-2121-6-17-S5.ogv ‎(Ogg Theora video file, length 4.0 s, 256 × 255 pixels, 1.94 Mbps, file size: 949 KB)

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English: Additional File 5 Perinuclear EB1-ΔN2-GFP aggregate assembly is microtubule-dependent. Image capture rate was 1 frame/10s using a 63X oil immersion lens, playback rate is 20 frames/s. Cells were incubated in nocodazole for 4 h followed by a wash and the addition of fresh imaging medium without drug. Imaging was initiated 30 min after nocodazole wash out. In the absence of drug EB1-ΔN2-GFP aggregates regain motility. Movement is intermittent and with an overall retrograde bias leading to the growth of perinuclear aggregates.
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Source Riess N, Milward K, Lee T, Adams M, Askham J, Morrison E (2005). "Trapping of normal EB1 ligands in aggresomes formed by an EB1 deletion mutant". BMC Cell Biology. DOI:10.1186/1471-2121-6-17. PMID 15813965. PMC: 1090566.
Author Riess N, Milward K, Lee T, Adams M, Askham J, Morrison E
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Format Bitrate Download Status Encode time
VP9 240P 314 kbps Completed 02:45, 24 October 2018 5.0 s
Streaming 240p (VP9) 315 kbps Completed 00:10, 21 December 2023 1.0 s
WebM 360P 493 kbps Completed 18:33, 2 December 2023 1.0 s
Streaming 144p (MJPEG) 1.01 Mbps Completed 13:46, 10 November 2023 0.0 s

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