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Fig. 6. RhoGEF2 and Dia localisation at the furrow canal do not depend on microfilaments. Permeabilized wild-type (A,B) embryos or (C) embryos with a GFP-moesin transgene were incubated with (A) buffer or (B,C) latrunculin A (LatA) to inhibit actin polymerisation, and stained for DNA (blue), F-actin (green); (A,B) RhoGEF2 and Dia; (C) GFP fluorescence. Scale bar: 50 µm.





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