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. 2015 Jun 9;6:259. doi: 10.3389/fimmu.2015.00259

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Copyright © 2015 Tseng, Arasteh, Kaur, Kozlowska, Topchyan and Jewett.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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MHC class-I, B7H1 and CD54 surface receptor analysis on wild type and COX-2 knockout MEFs. The surface expression of MHC class-I (A), B7H1 (B), and CD54 (C) on wild type and COX-2 knockout MEFs were assessed using staining with PE-conjugated antibodies followed by flow cytometric analysis. The surface expression of Rae-1γ on wild type and COX-2 knockout MEFs was assessed using staining with PE-conjugated antibodies followed by flow cytometric analysis (D). Isotype control antibody was used as control. One of four experiments is shown.

MHC class-I, B7H1 and CD54 surface receptor analysis on wild type and COX-2 knockout MEFs. The surface expression of MHC class-I (A), B7H1 (B), and CD54 (C) on wild type and COX-2 knockout MEFs were assessed using staining with PE-conjugated antibodies followed by flow cytometric analysis. The surface expression of Rae-1γ on wild type and COX-2 knockout MEFs was assessed using staining with PE-conjugated antibodies followed by flow cytometric analysis (D). Isotype control antibody was used as control. One of four experiments is shown.