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. 2016 Jan 8;5(5):e1128613. doi: 10.1080/2162402X.2015.1128613

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© 2016 The Author(s). Published with license by Taylor & Francis Group, LLC

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

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Figure 2. — Mouse cripto-1 peptides bind to H2-Kb in vitro and in silico. (A) RMA-s cells were used to measure surface stabilization of H2-K^b using an overlapping 15-mer peptides library. H2-K^b was analyzed by flow cytometery after loading with 100 µg/mL of peptide for 2 h, with negative controls (un-stained, filled gray, and un-load, green), positive controls (OVA and TRP2, red) as well as the peptides mCR_46-60, mCR_16-30, mCR_1-15 (solid black). (B) 9mers within Cripto-1 were identified using in silico prediction analysis with NetMHC.