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CXCL13 induces JNK activation through DOCK2 in PC3 cells. RWPE‐1, LNCaP and PC3 cells were treated with DOCK2 siRNA and corresponding controls (2 μm) in the presence or absence of CXCL13 (100 ng/ml). Lysates were collected 5 min following CXCL13 stimulation and samples were resolved on SDS–PAGE. Membranes were blotted for phospho‐JNK (46 kDa). GAPDH serves as loading control.
