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. Author manuscript; available in PMC: 2018 Jun 4.
Published in final edited form as: J Cell Physiol. 2011 Oct;226(10):2555–2561. doi: 10.1002/jcp.22602

Fig. 6.

Fig. 6

Part A: A Western blot showing pY416 SFK-immunoreactive band density in the epithelium of intact lenses that had been exposed for 15 min to ET-1 (100 nM) in the presence or absence of the SFK inhibitor PP2 (10 μM) added 45 min prior to ET-1. Some lenses received PP2 alone. Control lenses received neither ET-1 nor PP2. β-actin served as a loading control. Part B: Pooled data on pY416 SFK band density relative to β-actin band density. The values are the mean ± SE of results from three independent experiments. ***P < 0.001 indicates a significant difference from the control and ##P < 0.01 indicates a significant difference from ET-1 treatment.