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. 2022 Sep 8;18(11):1270–1276. doi: 10.1038/s41589-022-01140-1

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 8 — (A) Relative hFc-ACE2 binding to SARS-CoV-2 spike protein which has been pre-associated with 200 nM CV10-2449-XMAb (left) or the TEV cleaved form (right). No competitor was set to a value of 1.0. (B) The CrossMAb IgG ReconnAb binds to FcγRI, CrossMAb IgG was loaded on the octet using FAB2G tips and then associated with human FcγRI at 200 nM. The results demonstrate specific binding at an appropriate affinity.