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. 1999 Nov 1;147(3):619–630. doi: 10.1083/jcb.147.3.619

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© 1999 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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Intracellular translocation of pp125^FAK cleavage fragments to the cytoplasm. SMC cultured on monomeric collagen in the presence (+) or absence (−) of degraded collagen (Deg. Col.) fragments were lysed with Triton X-100 lysis buffer and fractionated into Triton X-100–soluble (cytoplasmic) and –insoluble (cytoskeletal) extracts. Extracts were then separated by SDS-PAGE, transferred to a membrane, and immunoblotted with ^2-18N-pp125^FAK antibodies.