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. 2014 Sep 26;33(21):2581–2596. doi: 10.15252/embj.201488351

Figure 2. Map3k1mPHD ES cells exhibit defective JNK and p38 activation following TGF-β, EGF and nocodazole stimulation.

Figure 2

A–D WT and Map3k1mPHD ES cells were kept on low serum and stimulated with (A) TGF-β (10 ng/ml), (B) EGF (100 ng/ml), (C) sorbitol (500 mM) or (D) nocodazole (0.5 μg/ml) for 10, 30 and 60 min or left unstimulated. Cells were lysed and analysed by IB using the indicated antibodies.

Data information: Results are representative of three independent experiments.

Source data are available online for this figure.