Figure 1
Figure 1. Expression and distribution of WAVE1 and WAVE2 in fibrinogen- and collagen-adherent MKs derived from ES cells. On day 12 of the differentiation protocol, MKs were plated onto 100 μg/mL fibrinogen, or onto 10 μg/mL collagen I, and allowed to stand for 60 minutes. Cells were fixed, permeabilized, and stained with rhodamine-conjugated phalloidin to mark F-actin (red) and with anti-WAVE1 or anti-WAVE2 antibodies followed by Alexa 488 (green), and analyzed by confocal microscopy. Scale bar equals 10 μm. See “Image acquisition for platelet and MK spreading” for complete image acquisition information.

Expression and distribution of WAVE1 and WAVE2 in fibrinogen- and collagen-adherent MKs derived from ES cells. On day 12 of the differentiation protocol, MKs were plated onto 100 μg/mL fibrinogen, or onto 10 μg/mL collagen I, and allowed to stand for 60 minutes. Cells were fixed, permeabilized, and stained with rhodamine-conjugated phalloidin to mark F-actin (red) and with anti-WAVE1 or anti-WAVE2 antibodies followed by Alexa 488 (green), and analyzed by confocal microscopy. Scale bar equals 10 μm. See “Image acquisition for platelet and MK spreading” for complete image acquisition information.

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