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. 2011 Nov 15;22(22):4373–4379. doi: 10.1091/mbc.E11-03-0219

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© 2011 Halbsgut 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: — Dividing larval neuroblasts mutant for different vesicle-trafficking genes do not exhibit polarity defects. Larval neuroblasts in wild-type (A) and mutant (B–K) MARCM clones were stained for aPKC (red), Mira (blue), GFP, and phospho-histone H3 (both in green). The genotype of the mutant clones is indicated. CD8::GFP (green) marks the homozygous mutant cells. Scale bar, 10 μm. DNA is stained with DAPI (turquoise).