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. 2020 Jan 10;14(2):387–406. doi: 10.1002/1878-0261.12626

Figure 4.

Figure 4

SNX16 interacts with eEF1A2 in CRC. (A, B). The proteins pulled down by using anti‐SNX16 and IgG were visualized by silver staining. Co‐IP of SNX16‐binding proteins followed by mass spectrometry led to the identification eEF1A2 as a SNX16‐binding protein. (C) The protein–protein interactions between SNX16 and eEF1A2 were confirmed by Co‐IP in HT29 and LoVo cells. (D) IF analyses of colocalization of SNX16 (green) and eEF1A2 (red) in HT29 and LoVo cells (left). The quantitative values of the colocalization of SNX16 and eEF1A2 (right). The scale bars represent 10 µm.