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. 2011 May;178(5):1986–1998. doi: 10.1016/j.ajpath.2011.01.021

Figure 1.

Figure 1

Acquisition and treatment of the TMA double labeled by immunofluorescence for p53 and HIPK2. A: Low-resolution acquisition of the overall TMA. B: Confocal microscopy acquisition of three fluorescent signals: DAPI (nuclear staining), p53 (green Alexa 488), and HIPK2 (red Alexa 594) of a single core. C: Operator-guided microdissection of images to eliminate stromal component. D: Segmentation and threshold-based cell scoring.