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. 2011 Apr 29;6(4):e19245. doi: 10.1371/journal.pone.0019245

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Ryu 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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A. Kinetic analysis of the LILRB2 D1D2 monomer binding to the immobilized HLA-A*0201 (as a positive control). Protein at the indicated concentrations was injected through the HLA-A*0201-immobillzed flow cells (700 response units (RU)). B. Kinetic analysis of the LILRB2 D1D2 monomer binding to the immobilized HLA-G1 (as a positive control). Protein at the indicated concentrations was injected through the HLA-G1-immobilized flow cells (300 RU). C. Kinetic analysis of the LILRA3 D1D2 monomer binding to immobilized HLA-A*0201. D. Kinetic analysis of the LILRA3 D1D2 monomer binding to immobilized HLA-G1. E. Kinetic analysis of the LILRA3 D1 monomer binding to immobilized HLA-A*0201. F. Kinetic analysis of the LILRA3 D1 monomer binding to immobilized HLA-G1.