Fig. 4.
Localization and translocation of PLCγ2 and Btk in XID megakaryocytes.
XID mouse megakaryocytes were stimulated by CRP (4 μg/mL; 90 seconds) and stained for PLCγ2 and Btk. Cells were analyzed by fluorescence microscopy and deconvolution as described in Figure 1. Scale bar = 20 μm. Each image is representative of 7 megakaryocytes obtained from a minimum of 3 experiments on different animals.