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Figure 1: Growth inhibition of human multiple myeloma cells by lidamycin (LDM). Cells were exposed to LDM for 48 h and determined by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium). Data are from three independent experiments

Figure 1: Growth inhibition of human multiple myeloma cells by lidamycin (LDM). Cells were exposed to LDM for 48 h and determined by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium). Data are from three independent experiments