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. 2016 May 6;11(5):e0154342. doi: 10.1371/journal.pone.0154342

Fig 2. Functional analysis of platelets from Gata1cKOMK and SykcKOMK mice show overlapping defects.

Fig 2

(a) Flow cytometry-based platelet aggregation assay (FCA) shows the aggregation capacity of platelets when stimulated with different agonists. Gata1cKOMK and WTlox platelets were studied. PMA, phorbol myristate acid; Agg, aggretin; Botro. Botrocetin; Coll, collagen; CVX, convulxin. (b) MFI of receptors expressed on Gata1cKOMKplatelets, relative expression of a given receptor in WTlox platelets was set to 100. For clarification: CD61 (Itgb3), CD41 (Itga2b), CD42a (GPIX), CD42b (Gp1ba), CD42c (Gp1bb), CD49b (Itga2). (c) Flow cytometry-based platelet aggregation assay (FCA) shows the aggregation capacity of SykcKOMK and WTlox platelets when stimulated with various agonists as described above.