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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 B) and primary monocytes (C and D) were incubated with medium alone (A and C) or 10 μg/ml cNK-2 (B and D) for 30 min at 41 °C. Immunocytochemistry was performed with a rabbit polyclonal cNK-2 (green) antibody followed by an Alexa Fluor 488 goat anti-rabbit IgG secondary antibody. DAPI and Alexa Fluor 555 Phalloidin were used to stain nuclei (blue) and F-actin (red), respectively. The scale bar in all figures corresponds to 20 μm.