HEL cells, treated with 25 μM of G6 for 0 or 24 h, were analyzed via indirect immunofluorescence for changes in the cellular distribution of vimentin and β-actin in response to drug treatment. Vimentin (A and B) and β-actin (G and H) were indirectly labeled with a FITC-conjugated secondary antibody. The nuclei were counter stained with DAPI (C, D and I, J). The images were then merged (E, F and K, L). Shown is one of two representative results.