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. 2018 May 29;9(6):654. doi: 10.1038/s41419-018-0695-6

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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. 7 — a Immunoprecipitation and silver staining was performed by using the whole proteins SW480 cells with anti-FSTL1 antibody. b The spectrogram of differential protein band is identified as VIM (Quadrupole Mass Spectrometer). c Coimmunoprecipitations were performed to validate the interaction among FSTL1, VIM, and FAK in SW480 cells. d FSTL1 (red, upper panel) or FAK (red, lower panel) co-localizate with VIM (green) in RKO and DLD1 cells was assessed by laser-scanning confocal microscopy, respectively (×1800, scale = 10 μm). DAPI (blue) stains nuclei. The image in white pane of the upper right corner of overlay is a partial enlarged detail. Error bars in the histogram represent the mean ± S.D. of the colocalisation coefficients of VIM and FSTL1 (upper panel) or the colocalisation coefficients of VIM and FAK (lower panel) in RKO cells and DLD1 cells (n = 10)