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. 1999 Aug 9;146(3):673–682. doi: 10.1083/jcb.146.3.673

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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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Binding of mAb 10G2 to IAP. Top, OV10 cells expressing IAP, IAP/GPI, or IAP/CD7 were incubated with the mAb 10G2. FACS^® analysis with anti-IAP mAb B6H12 showed that both IAP/GPI and IAP/CD7 were expressed at a level at least equivalent to that of wild-type IAP (mean channel fluorescence wild-type IAP, 3.8 ± 0.1; IAP/GPI, 6.1 ± 0.3; IAP/CD7, 11.7 ± 1.4; Lindberg et al. 1996b; data not shown). Middle, 10G2 binding was determined on buffer-treated OV10, cholesterol-depleted OV10, and cholesterol-repleted OV10 expressing wild-type IAP. Bottom, Binding of conventional anti-IAP mAb 2D3 and 2B7 (Brown et al. 1990) was determined on buffer-treated and MβCD-treated OV10 expressing wild-type IAP.