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. 2000 Feb 7;148(3):579–590. doi: 10.1083/jcb.148.3.579

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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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Schematic representation of N-cadherin wild-type and mutated constructs and coimmunoprecipitation experiments. A, The constructs of wild-type N-cadherin (NWT), EC1 domain deletion (NΔEC1), Trp-2 mutated to Ala in N-cadherin (NW2A), and a chimeric molecule of E-cadherin whose EC1 domain was replaced by the N-cadherin EC1 domain (ENEC1). B, Western blot analysis of lysates and immunoprecipitates from L_R/N, L_R/NΔEC1, and L_R/NW2A cells. C, Four L_R/NW2A clones expressing different levels of R- and N-cadherin (NW2A) were detected, and then immunoprecipitated by GFP antibody and analyzed by immunoblotting.