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. 2010 Jan 18;207(1):77–84. doi: 10.1084/jem.20091097

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© 2010 DeBusk et al.

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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Figure 1. — δ-Catenin is expressed in vascular endothelium. (A) Protein lysates collected from neuronal cells (HT-22 and U251 MG), endothelial cells (ECs; HUVEC and HMEC), epithelial cells (293), and leukocytes (THP-1 and U937) were subjected to Western blot analysis and probed with a δ-catenin–specific antibody. (B) β-tubulin was used as a loading control. Immunofluorescent staining for δ-catenin was performed in cultured HUVECs. (C) Mouse skin tissue sections from wild-type and δ-catenin–null mice were analyzed by immunofluorescent double staining using antibodies against CD31 for endothelium, and δ-catenin. Nuclei were stained with DAPI. 400× magnification. Each experiment was repeated three times, and representative images were shown. Bar, 200 µm.