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. 2021 Jan 21;41(3):1092–1104. doi: 10.1161/ATVBAHA.120.315030

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© 2021 The Authors.

Arteriosclerosis, Thrombosis, and Vascular Biology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.

This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

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Figure 4. — Mapping GPVI (glycoprotein VI)-fibrinogen binding sites using microscale thermophoresis. Binding profiles of (A) X-fragment, (B) D-dimer, (C) D-fragment, and (D) E-fragment to fluorescein isothiocyanate (FITC)-dimeric GPVI at K_D of >2 μmol/L for X-fragment and >20 μmol/L for D-, E-fragment and D-dimer. K_D values were estimated as greater than the GPVI concentration that generates half of the maximum binding signal. All results are presented as mean±SD; N=3 for A–C and N=2 for D.