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. 2007 Jan 30;35(5):e32. doi: 10.1093/nar/gkl1171

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© 2007 The Author(s).

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 3. — Histograms from initial flow cytometric analyses of ExLib1 and ExLib2. Induced shake flask cultures were harvested after 4.5 h of induction and analyzed. (A) Analysis of ExLib1; (B) Analysis of previously isolated and here re-cultured ExLib1 subpopulations denoted low, medium and high (gates once used for the sorting are shown), cultured either in separate flasks (non-filled histograms) or together in a common flask (co-culture) (filled histogram); (C) Analysis of ExLib2; (D) Analysis of previously isolated and here re-cultured ExLib2 subpopulations denoted low, medium and high (gates once used for the sorting are shown), cultured either in separate flasks (non-filled histograms) or together in a common flask (co-culture) (filled histogram). The pre-amplifier gain was set to 799 V and the experiments were performed at least twice with similar results (data not shown).