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. 2010 Jun 7;207(6):1173–1182. doi: 10.1084/jem.20091318

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© 2010 Morita 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.rupress.org/terms). 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 1. — Markers with heterogeneous expression in CD34⁻KSL cells. KSL cells were stained with FITC-conjugated anti-CD34 antibody and additional PE-conjugated antibodies as shown. Shown are flow cytometric profiles for the markers that had heterogeneous expression within CD34⁻KSL cells (percentages are shown). Marker-positive or -negative cells were separated by using the sorting gates (shown as squares). In the case of CD150, CD34⁻KSL cells were separated into CD150^high, CD150^med, and CD150^neg fractions. In the case of CD38, CD34⁻KSL cells were separated into CD38^high and CD38^med fractions. The data represent four to eight independent experiments.