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. Author manuscript; available in PMC: 2013 Nov 25.
Published in final edited form as: Cell Prolif. 2011 Jun 6;44(4):10.1111/j.1365-2184.2011.00757.x. doi: 10.1111/j.1365-2184.2011.00757.x

Figure 4. CXCL13 induces JNK activation through DOCK2 in PC3 cells.

Figure 4

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.