Figure 1
Figure 1. Characterization of EphB2LacZ platelets. The presence of EphB2 (A), β-galactosidase (B), and ephrinB1 (C) was confirmed in control (a) and EphB2LacZ (b) mouse platelets by immunoblot analysis. Similarly, the expression level of P-selectin was measured in control (a) and EphB2LacZ (b) mouse platelets by immunoblot analysis (D). The expression levels of αIIbβ3 (E), α2β1 (F), GPVI (G), and GPIbα (H) were analyzed on control and EphB2LacZ platelets by flow cytometry. Data represent mean (of median fluorescence intensity) ± SD (n = 4, control and EphB2LacZ mice). (I) ephrinB1 was immunoprecipitated from control and EphB2LacZ platelets following stimulation with CRP-XL (0.5 µg/mL) and analyzed for its phosphorylation using anti-phosphotyrosine antibody by immunoblotting. The blots are representative of 3 separate experiments. CRP-XL, cross-linked collagen-related peptide; GP, glycoprotein; SD, standard deviation.

Characterization of EphB2LacZ platelets. The presence of EphB2 (A), β-galactosidase (B), and ephrinB1 (C) was confirmed in control (a) and EphB2LacZ (b) mouse platelets by immunoblot analysis. Similarly, the expression level of P-selectin was measured in control (a) and EphB2LacZ (b) mouse platelets by immunoblot analysis (D). The expression levels of αIIbβ3 (E), α2β1 (F), GPVI (G), and GPIbα (H) were analyzed on control and EphB2LacZ platelets by flow cytometry. Data represent mean (of median fluorescence intensity) ± SD (n = 4, control and EphB2LacZ mice). (I) ephrinB1 was immunoprecipitated from control and EphB2LacZ platelets following stimulation with CRP-XL (0.5 µg/mL) and analyzed for its phosphorylation using anti-phosphotyrosine antibody by immunoblotting. The blots are representative of 3 separate experiments. CRP-XL, cross-linked collagen-related peptide; GP, glycoprotein; SD, standard deviation.

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