Abstract
P. Ravichandran R. Gopikrishnan S. Biradar V. Goornavar G. T. Ramesh J. C. Hall (&) Molecular Toxicology Laboratory, Department of Biology, Center for Biotechnology & Biomedical Sciences, Norfolk State University, Norfolk, VA 23504, USA e-mail: jchall@nsu.edu Fig. 5 b LE cells were seeded equally and exposed to magnetite (1, 10, and 20 lg), cultured for 24 h and live and dead cells were visualized based on dye-uptake method and photographed. Dead cells were counted, and % of dead cells were calculated and shown below
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