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. 2012 Aug 20;7(8):e42792. doi: 10.1371/journal.pone.0042792

Figure 1. Nuclear Inline graphic-catenin during RVM cell differentiation.

Figure 1

(A) Representative Western-blot from which the Inline graphic-catenin protein amount was quantified (B). Time point 0 stands for control using proliferating cells and Inline graphic-actin was used as a loading control. The signal intensities at 0 hour are normalized to 1.0 and the values are presented as mean Inline graphic standard error on the mean from at least 3 independent experiments. The figure is reproduced from [12] (Figures 8C and 8D) where details about experimentation can be found, as well as in the section Materials & Methods.