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. 2017 Jan-Mar;13(49):21–24. doi: 10.4103/0973-1296.197645

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Copyright: © 2017 Pharmacognosy Magazine

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

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Effect of NJ_et on growth kinetics of neuroblastoma cells. (A) IMR-32 and (B) SK-N-MC cell lines were treated with NJ_et (0-20 μg/ml) for 24, 48 and 72 h and the number of viable cells were counted by trypan blue dye exclusion method. Data represent mean± SD of three independent experiments (C) IMR-32 and SK-N-MC cell lines were treated with NJ_et (0-20 μg/ml) and grown in soft agar for two weeks. Colonies were counted from at least 10 different areas and the average of each has been plotted. The data represents mean ± SD of five independent experiments.