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. 2015 Nov 24;10(11):e0143449. doi: 10.1371/journal.pone.0143449

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© 2015 Paletta 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 properly credited.

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Fig 1 — (A) α1 and α2 domain amino acids of CD1d molecules used in this study. Alignment was performed using BioEdit. Human: GenBank BC027926.1, Mouse: GenBank AK002582.1, Rat: GenBank AB029486.1, Cotton Rat: GenBank KM_267558. (B) In vitro loading analysis of CD1d dimers presented as schematic overview. (C) Scheme explaining the emergence of different saturating curves depending on loading efficacy of dimers. Upper panel: Inefficient loading leads to low proportion of functionally bivalent CD1d dimers, Lower panel: Efficient loading leads to high proportion of functional bivalent CD1d dimers. Drawing represents several step flow cytometry analysis of incubation/wash/detection. (D) Structural features of all glycolipids used in this study.