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Fig. 5. Fibronectin-stimulated tyrosine phosphorylation of PLC-{gamma}1. (A) Null+ cells were allowed to adhere to fibronectin-coated dishes (10 µg ml-1) in serum-free medium for the indicated times. The cells were then lysed and each lysate was precipitated with anti-PLC-{gamma}1 antibody followed by blotting with site-specific antibodies against tyrosine-phosphorylated-PLC-{gamma}1 or PLC-{gamma}1 as indicated. (B) Null+ cells expressing wild-type PLC-{gamma}1 or an N+C-SH2-domain loss-of-function PLC-{gamma}1 mutant (N+C SH2-) (Ji et al., 1999) were allowed to adhere to fibronectin (10 µg ml-1) for the indicated times. The cells were than lysed and the lysate were precipitated with anti-PLC-{gamma}1 antibody and then blotted with antibody against tyrosine-783-phosphorylated PLC-{gamma}1 or PLC-{gamma}1 as indicated. Cells maintained in suspension (Susp) were used as a control for time 0.





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