Fig. 5.
Fig. 5. Autokinase assay and phosphorylation on tyrosine of the CEP110-FGFR1 fusion protein. / NIH3T3 cells transiently transfected by either CEP110-FGFR1 cDNA (CEP110-FGFR1) or the empty vector (pcDNA3) and FGFR1 overexpressing cells (NFlg26) were cultured in the presence (+) or absence (−) of FGF1 plus heparin. Immunoprecipitates using anti-C-FGFR1 antibody were analyzed for autokinase activity (left panel) (autoradiography of 4 hours for all samples) and phosphorylation on tyrosine after Western blot with anti-phosphotyrosine antibody 4G10 (right panel). The position of molecular mass standards (in kd) is indicated.

Autokinase assay and phosphorylation on tyrosine of the CEP110-FGFR1 fusion protein.

NIH3T3 cells transiently transfected by either CEP110-FGFR1 cDNA (CEP110-FGFR1) or the empty vector (pcDNA3) and FGFR1 overexpressing cells (NFlg26) were cultured in the presence (+) or absence (−) of FGF1 plus heparin. Immunoprecipitates using anti-C-FGFR1 antibody were analyzed for autokinase activity (left panel) (autoradiography of 4 hours for all samples) and phosphorylation on tyrosine after Western blot with anti-phosphotyrosine antibody 4G10 (right panel). The position of molecular mass standards (in kd) is indicated.

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