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. 2014 May 13;9(5):e97432. doi: 10.1371/journal.pone.0097432

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© 2014 Elliott et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) HT29 LM1, LM2, LM3 and parental cell line were cultured in normal medium for 24 h. Protein expression profiles were analyzed by Western blot. β-actin was used as a loading control. (B) IHC analysis of CD44 and p-MET expression in HT29 LM1 and HT29 LM3 liver metastasis tissue sections. (C) Flow cytometry analysis of CD44 geometric mean fluorescence intensity in parental HT29 and HT29 LM3 cells.