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Fig. 2. Dual labeling of the FN matrix with FN-yfp and the actin cytoskeleton with
cfp-Moe. Cells were cultured for 48 hours to allow matrix assembly and stained
with polyclonal antibody for FN (c) or with phalloidin for actin (e). (a, b
and d) show the fluorescence of yfp and cfp as indicated, and in (f), the yfp
and cfp images are superimposed. Bar, 50 µm.
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