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. 2017 Mar 23;7:45099. doi: 10.1038/srep45099

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Copyright © 2017, The Author(s)

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HD11 cells (A) and primary monocytes (B) were incubated with 10 μg/ml cNK-2 and 1 μg/ml E. coli LPS. RNA was isolated after 4 h and used for real-time qPCR in triplicate. (C) The induction of NO production by E. coli LPS alone or in the presence of cNK-2 was determined by a Griess assay. The data represent the mean ± SE from two or three independent experiments. p < 0.01 (**) and p < 0.001 (***) were considered statistically significant compared to the medium control.