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. 2011 Mar 1;2:123–131. doi: 10.7150/jca.2.123

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© Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.

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Fig 1 — In vitro characterization of LMB-H226-GL cells. A. FACS analysis showing GFP fluorescence in the LMB-H226-GL cell line. Shaded area: parental NCI-H226; heavy solid line: LMB-H226-GL. B. Mesothelin expression on LMB-H226-GL. Shaded area: NCI-H226 without anti-mesothelin staining; thin dotted line: LMB-H226-GL without staining; heavy solid line: NCI-H226 with staining; heavy dotted line: LMB-H226-GL with staining. C. WST-8 assay of NCI-H226 and LMB-H226-GL. Various amounts of SS1P immunotoxin were used to treat NCI-H226 and LMB-H226-GL cells.