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ARHGAP24 was downregulated in BC tissues. Thirty BC tissue samples and the paired adjacent tissues were used to detect the expression of ARHGAP24. (A) qRT-PCR results of ARHGAP24 mRNA levels normalized to GAPDH. (B) Western blot results of ARHGAP24 protein levels. GAPDH was used as the loading control. T1–4, tumor tissues; A1–4, BC adjacent tissues. (C) Statistical analysis of the relative protein levels of ARHGAP24. ** P<0.01, *** P<0.001 compared with adjacent tissues.
