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Fig. 3. Analysis of the effects of PTP inhibition on STATc tyrosine
phosphorylation. (A) Induction assay using dominant-negative forms
of PTP3 cells transformed with myc:PTP3
CS were starved in suspension
for 4 hours and then exposed to DIF-1 at 100 nM. The activation of STATc was
analysed by western transfer using an antibody specific to the tyrosine
phosphorylated form of STATc. As a loading control, a parallel blot was probed
with a non phospho-specific STATc antibody. (B) Pervanadate-mediated
inhibition of PTP3 Ax-2 cells. Cells were starved in suspension for 4 hours,
then exposed to DIF-1 at 100 nM or pervanadate at 2 mM (1 mM
H2O2 and 2 mM NaVO4) for the indicated times
and analysed as in A.