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. 2004 Jun;15(6):2558–2567. doi: 10.1091/mbc.E03-09-0700

Figure 6.

Figure 6.

Tyrosine phosphorylation of FAK in GD25-β1A and GD25-β1AK756L cells after β1-mediated adhesion. FAK was immunoprecipitated from cells kept in suspension (S), or plated on LN-1 or anti-β1 mAb Ha2/5 (Ab) for 1 h. Immunoprecipitated material was separated by SDS-PAGE, transferred to nitrocellulose filters, and the filters were probed for phosphotyrosine (A and B) and for FAK phosphotyrosine-397 by using site-specific antibody (C). After stripping, the filters were reprobed with anti-FAK mAb as a loading control.