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. 1999 Mar;19(3):2416–2424. doi: 10.1128/mcb.19.3.2416

FIG. 3.

FIG. 3

Increased tyrosine phosphorylation of Stat1,2 and Jak1 by IFNs in Shp-2−/− cells. Serum-starved wild-type and Shp-2−/− cells were treated with 100 ng of IFN-γ/ml (A) or 1,000 U of IFN-α/ml (B and C) for the indicated time periods. Whole cell extracts (A and B) or anti-Stat2 immunoprecipitates (C) were subjected to SDS-polyacrylamide gel electrophoresis and subsequently to immunoblot analyses with anti-PY, anti-PY-Stat1, anti-Stat1, or anti-Stat2 antibodies as indicated. (D) Serum-starved wild-type and Shp-2−/− cells were treated with 100 ng of IFN-γ/ml for the indicated time periods. Whole cell extracts were immunoprecipitated with anti-Jak1 antibody and subjected to immunoblot analyses with anti-PY and anti-Jak1 antibodies as indicated.