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. 2004 Jun;24(12):5353–5368. doi: 10.1128/MCB.24.12.5353-5368.2004

FIG. 8.

FIG. 8.

KAKTLR is defective for signaling in vivo. (A) Lysates of CE cells expressing empty RCAS A (lanes 1 and 2), FAK (lanes 3 and 4), or KAKTLR (lanes 5 and 6) were analyzed by Western blotting for phosphotyrosine (pTyr). Prior to lysis, cells were either left untreated or treated with 50 μM vanadate (VO4) for 16 h. (B) Endogenous paxillin was immunoprecipitated from lysates of control cells (lanes 1 and 2) or cells expressing FAK (lanes 3 and 4) or KAKTLR (lanes 5 and 6) treated as for panel A. Tyrosine phosphorylation was examined by Western blotting (top). The blot was stripped and reprobed with a monoclonal antibody recognizing paxillin (bottom).