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. 2017 May 11;8(34):57907–57933. doi: 10.18632/oncotarget.17826

Figure 7. The effect of C1orf64 on AR promoter binding and the interaction between C1orf64 and AR.

Figure 7

(A) Fold enrichments of ChIP for PIP promoter performed with an AR antibody (AR-Ab) following the transfections of control (CT)-siRNA or C1orf64-siRNA (Duplex 1) in T-47D cells. AR binding to each promoter region (A1-A4) was assessed. Amplification of 1% of input chromatin was used as the input control and a non-specific antibody served as negative control (dashed-line). *, p< 0.03 is for C1orf64-siRNA vs. CT-siRNA in A1 and A2. Error Bars: ± 2SEM. (B) Co-immunprecipitation assays (Co-IP) to investigate the interaction between endogenous C1orf64 and AR in T-47D and MFM-223 cell lines. AR-IP was performed using an AR antibody and control experiments were conducted with a non-specific rabbit IgG. Immunoblot analysis were carried out on IP supernatants using C1orf64 and AR antibodies. Input was assessed with AR immunoblotting on 5% of lysates collected before each IP. All co-IP experiments were performed in three replicates.