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. 2015 Apr 17;10(4):e0124237. doi: 10.1371/journal.pone.0124237

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© 2015 Guan 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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Fig 1 — (A) Western blot analysis with β-tubulin used as loading control. (B) Immunofluorescence staining of NCAM and PSA-NCAM. ldlD-14 and ldlD/N140 cells were cultured in serum-free medium supplemented with 5% FBS or ITS or ITS+Gal, and nuclei were visualized by Hoechst staining. Size bars: 20 μm.