Fig. 4.
Fig. 4. Phosphopeptide inhibition of Stat3/β binding to hSIE. Whole-cell extracts (20 μg) of an acute leukemia cell line, EM2,28 stimulated with G-CSF (100 ng/mL) for 30 minutes were incubated with the indicated tyrosine phosphorylated peptides (+P) or nonphosphorylated peptides (−P) at 0, 30, 100, 300, and 400 μmol/L for 60 minutes at 37°C before addition of radiolabeled duplex hSIE and EMSA. The gels were dried and exposed to Kodak XAR film for before developing. The results shown are representative of three experiments.

Phosphopeptide inhibition of Stat3/β binding to hSIE. Whole-cell extracts (20 μg) of an acute leukemia cell line, EM2,28 stimulated with G-CSF (100 ng/mL) for 30 minutes were incubated with the indicated tyrosine phosphorylated peptides (+P) or nonphosphorylated peptides (−P) at 0, 30, 100, 300, and 400 μmol/L for 60 minutes at 37°C before addition of radiolabeled duplex hSIE and EMSA. The gels were dried and exposed to Kodak XAR film for before developing. The results shown are representative of three experiments.

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