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. 2014 Jul 1;25(13):2071–2083. doi: 10.1091/mbc.E14-01-0015

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© 2014 Xu et al. 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 3: — Characterization of phagosome maturation in cpl-1 mutants. Representative images of cell corpse labeling by CED-1::GFP (A), GFP::moesin (B), GFP::RAB-5 (C), YFP::2xFYVE (D), GFP::RAB-7 (E), and LST-4::GFP (F). Cell corpses are indicated by arrows. Bars, 5 μm. (G) Quantification of the labeling of cell corpses by different phagosomal markers shown in A–F. We analyzed ≥100 cell corpses from ≥20 animals for each marker, and data were derived from three repeats. Comparisons were performed between N2 and cpl-1(yq89) mutants for each marker using an unpaired t test. All points have p > 0.05.