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. 2009 Jun 15;185(6):995–1012. doi: 10.1083/jcb.200903125

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© 2009 Nishihama et al.

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.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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Figure 2. — Localization of Inn1 to the bud neck at mitotic exit in wild-type and AMR-deficient cells. (A and B) Strains LY1302 (INN1-GFP; A) and YEF5293 (myo1Δ INN1-GFP; B) were transformed with plasmid YCp111-CDC3-CFP and observed by time-lapse microscopy (Videos 1–4). (C) Wild-type (WT; RNY2395) and iqg1Δ (RNY2393) cells expressing Inn1-GFP and containing plasmid YCp50-IQG1 were grown overnight at 25°C on an SC+FOA plate to eliminate the plasmid, were scraped from the plate, and imaged by DIC and fluorescence microscopy. Bars, 2 µm.