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. 2018 Feb 20;9(3):292. doi: 10.1038/s41419-017-0253-7

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — a EGF-induced CaM colocalization with Src in the cytoplasma by Immunofluorescence analysis. Green: CaM, Red: Src, Blue: Nucleus. (Representative images were presented. Images were taken from three different microscopic visions from every independent experiment). b EGF-induced CaM colocalization with NHE1 in the cytoplasma by Immunofluorescence analysis. Green: CaM, Red: Src, Blue: Nucleus. (Representative images were presented. Images were taken from three different microscopic visions from every independent experiment). c The distribution of CaM in nucleus and cytoplasm with different concentrations of EGF were detected by western blot. Lamin B1 and GAPDH served as nucleus (Nuc) and cytoplasmic (Cyto) loading control, respectively. d The combination between CaM and Src/NHE1 was detected by using co-immunoprecipitation assay without treatment with EGF. e Upon treatments with different concentrations of EGF, the binding of CaM with Src and NHE1 was explored by co-immunopreciptation