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. 2006 Jul;5(7):1136–1146. doi: 10.1128/EC.00383-05

FIG.1.

FIG.1.

Identification of EppA by 2-D electrophoresis of 32P-labeled cells. (A) Coomassie brilliant blue-stained 2-D gels of wild-type and Dderk2 cells before and 1 min after stimulation with cAMP. The box in the wild-type 1-min sample is shown at higher magnification in panel C. Black squares in diagonally opposite corners are filter papers containing 32P for registration of the autoradiograms in panel B. (B) Autoradiography of 2-D gels in panel A. Phosphoproteins present in three experiments and quantitated in Table 1 are labeled in the autoradiogram of the stimulated wild-type sample. (C) DdERK2-dependent protein position shift and phosphorylation change of EppA. The arrowhead points to the position of phosphorylated EppA (spot 3 in Fig. 1B), and arrows indicate the corresponding position in samples from unstimulated or DdErk2 cells.