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. 2010 Feb 1;25(7):2107–2119. doi: 10.1093/ndt/gfq006

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© The Author 2010. Published by Oxford University Press [on behalf of the ERA-EDTA]. All rights reserved. This is an Open Access article of the Creative Commons Attribution License (http://creativecommons.org/licenses?by-nc/2.0/uk) which permits unres distribution, and reproduction in any medium, provided the original work is properly cited.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5),which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 6 — Localization of claudin-3, -4 -7 and -8 compared to aquaporin-2 and calbindin: photomicrographs showing serial sections of human renal cortical tissue stained for claudin-3 (A), claudin-4 (B), aquaporin-2 (C), calbindin (D), claudin-8 (E) and claudin-7 (F) [claudin-3, -4, -8 and -7 stained tubules that were coincident with similar ones that were positive for aquaporin-2 and calbindin (asterisks in A–F) but were also localized in calbindin positive, aquaporin-2 negative tubules (arrowheads in A–F); claudin-4, -7 and -8 showed similar staining patterns, whereas claudin-3 strongly stained additional tubules which were negative for claudin-4, -7, -8, aquaporin-2 and calbindin (arrows in A–F); scale bar 100 µm].