Figure 1.
Notch1 deficiency reduces the number of circulating platelet and TPO production. (A) Peripheral blood was drawn to measure the number of circulating platelets by an automatic blood analyzer (mean; n = 17; unpaired student t test). (B) Notch1fl/fl or HC Notch1−/− mice received intraperitoneal administration of rat anti-mouse integrin GPIIb/CD41 immunoglobulin at a dose of 0.1 mg/kg, followed by monitoring the number of circulating platelets at different time points (mean ± standard error of the mean [SE]; n = 7; 2-way analysis of variance [ANOVA]). Plasma (C) or liver mRNA (D) was isolated from Notch1fl/fl or HC Notch1−/− mice to measure TPO level by ELISA (mean ± SE; n = 3) or quantitative real-time PCR (mean ± SE; n = 8; unpaired student t test). ∗P < .05; ∗∗P < .01; ∗∗∗P < .001; ∗∗∗∗P < .0001. ELISA, enzyme-linked immunosorbent assay; PCR, polymerase chain reaction.

Notch1 deficiency reduces the number of circulating platelet and TPO production. (A) Peripheral blood was drawn to measure the number of circulating platelets by an automatic blood analyzer (mean; n = 17; unpaired student t test). (B) Notch1fl/fl or HC Notch1/ mice received intraperitoneal administration of rat anti-mouse integrin GPIIb/CD41 immunoglobulin at a dose of 0.1 mg/kg, followed by monitoring the number of circulating platelets at different time points (mean ± standard error of the mean [SE]; n = 7; 2-way analysis of variance [ANOVA]). Plasma (C) or liver mRNA (D) was isolated from Notch1fl/fl or HC Notch1/ mice to measure TPO level by ELISA (mean ± SE; n = 3) or quantitative real-time PCR (mean ± SE; n = 8; unpaired student t test). ∗P < .05; ∗∗P < .01; ∗∗∗P < .001; ∗∗∗∗P < .0001. ELISA, enzyme-linked immunosorbent assay; PCR, polymerase chain reaction.

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