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. 2013 Mar 1;24(5):643–658. doi: 10.1091/mbc.E12-09-0659

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© 2013 Baetz and Goldenring. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 6: — FIP1A overlaps with FIP1B and FIP1C along tubular compartments. Time-lapse imaging of mCherry-FIP1A with EGFP-FIP1B (Supplemental Video S5) or EGFP-FIP1C (Supplemental Video S6) in live HeLa cells conducted over 2 min. (A) FIP1B on tubular compartments with FIP1A. The insets show an example tubule compartment labeled with both mCherry-FIP1A and EGFP-FIP1B moving from the perinuclear region to the periphery of the cell. (B) EGFP-FIP1C and mCherry-FIP1A along tubular compartments that move in the same direction and change directions together. Insets highlight the overlap along the compartment and the movement of an example tubule. Data represent at least three independent experiments. Bars, 10 μm.