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.