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. 2017 Jul 1;26(13):964–972. doi: 10.1089/scd.2017.0017

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© Cristina L. Esteves et al. 2017; Published by Mary Ann Liebert, Inc.

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 work is properly cited.

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FIG. 1. — IHC of equine AT sections showing staining for the pericyte markers, CD146 (A), NG2 (B), αSMA (C), and the MSC markers, CD29 (D) and CD90 (E). CD144 was used as endothelial marker (red; A, B, D, E). Colocalization of pericyte (NG2 and CD146) and MSC markers (CD146 and CD73; F, G, respectively) in yellow (left panel) from the overlap of green (middle panel) and red (right panel) individual antibody fluorescence. DAPI was used to stain nuclei. Scale bar, 10 μm, is indicated by white bars. IHC, immunohistochemistry; MSC, mesenchymal stem/stromal cell. Color images available online at www.liebertpub.com/scd