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. 2016 Jun 3;7(26):39396–39407. doi: 10.18632/oncotarget.9818

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Copyright: © 2016 Omar et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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A. Flow cytometry analysis of the staining for CD122 (IL-2Rβ) and CD44 in splenic CD8⁺ T cells from C57BL6/J, Slfn2^eka/eka, CHOP^−/− /Slfn2^eka/eka or XBP1^lox/lox /Slfn2^eka/eka mice (n =9). Numbers in quadrants indicate percent cells in each. B., C. Flow cytometry analysis for the expression levels of CD62L (upper panel) and IL-7Rα (CD127) (lower panel) on surface of both CD8⁺CD44^lo (left) and CD8⁺CD44^hi (right) T cells from the C57BL6/J, Slfn2^eka/eka, CHOP^−/− /Slfn2^eka/eka (B) or XBP1^lox/lox /Slfn2^eka/eka mice (C) (n=9).