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. 2000 Sep 4;150(5):1209–1214. doi: 10.1083/jcb.150.5.1209

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© 2000 The Rockefeller University Press

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.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

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Dystrophin and F-actin colocalize on mechanically isolated sarcolemma in a costameric pattern. Shown is a mechanically isolated sarcolemma (a), or a skinned myofiber (b) both stained with Alexa488-phalloidin (green) and rabbit 2 antiserum to dystrophin (red). Red and green channels were collected simultaneously and areas of coincidence appear yellow. Shown on the left in (c) are immunoblots containing WGA-Sepharose eluates from detergent solubilized control and mdx skeletal muscle membranes stained with rabbit 2 antiserum to dystrophin (Dys), or rabbit 56 antiserum to utrophin (Utr). Shown on the right in c are transverse cryosections of control and mdx skeletal muscle stained with rabbit 2 antiserum to dystrophin. Bars: (b) 10 μm; (c) 50 μm.