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. 2019 Jan 8;20:15. doi: 10.1186/s12864-018-5411-5

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Flow cytometric analysis of Bomac cells. Bomac cells were labeled with antibodies against CD14, CD16, CD11b, CD172a, CD44, MHC II, CD40, CD68, CD71, CCR2 and using single color staining. Another set of cells were stimulated with p(I:C) as described in Material and Methods, and then similarly stained for flow cytometry. At least 100,000 events were acquired in FACS Calibur flow cytometer and analyzed in FlowJo software. Results are shown as mean fluorescence intensity (MFI). Six separate stainings for each group of cells were performed. * = p ≤ 0.05