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. 2017 Aug 16;14(4):3720–3726. doi: 10.3892/etm.2017.4940

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Copyright: © Xu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 2. — Knockdown of TCTN1 expression in thyroid cancer cells by shTCTN1. (A) Representative pictures of green fluorescent protein (GFP) expression recorded under a fluorescence microscope in CAL62 and 8305C cells. (B) qRT-PCR analysis of TCTN1 mRNA levels in CAL62 and 8305C cells following shCon or shTCTN1 infection. Data are expressed as mean ± SD of 3 independent experiments. *P<0.05, ***P<0.001 vs. shCon. (C) Western blot analysis of TCTN1 protein levels in CAL62 and 8305C cells following shCon or shTCTN1 infection. The number in this figure indicated the relative expression of TCTN1 relative to GAPDH. GAPDH was used as an internal control.