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. Author manuscript; available in PMC: 2013 Jan 1.
Published in final edited form as: Cell Signal. 2011 Sep 3;24(1):140–150. doi: 10.1016/j.cellsig.2011.08.015

Figure 4.

Figure 4

Figure 4

A) Anti-EGFR and anti-HER2 immunofluorescence microscopy of the HER2 cells derived from the MCF-10A. Notable findings were efficient internalization of both EGFR and HER2, co-localization of EGFR and HER2, and reappearance of both proteins at the plasma membrane within 4 – 6 hours. B) Fluorescence intensity measurements of EGFR in the control and HER2 cells as well as HER2 in the HER2 cells of MCF10A origin. The bar graph represents mean ± standard deviation from three independent experiments.