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. Author manuscript; available in PMC: 2015 Nov 28.
Published in final edited form as: Cancer Lett. 2014 Aug 27;354(2):299–310. doi: 10.1016/j.canlet.2014.08.032

Fig. 7.

Fig. 7

Inhibition of cell migration by DJ4 is independent of cell death induction. (A) A549 cells were treated with various concentration of DJ4 for 24 h. Cells were further incubated with MTT and formazan crystals were dissolved in DMSO. Color intensity was measured by spectrophotometer. Cell viability of DJ4 treated cells was determined relative to vehicle treated controls. (B) A549 cells were treated for 24 h and stained with calcein and ethidium-homodimer. Live (calcein positive) and dead cells (ethidium-homodimer) were counted by flow cytometry.