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. 2020 Jun 15;136(15):1773–1782. doi: 10.1182/blood.2019003251

Figure 1.

Figure 1.

Generation and characterization of Rgs deletion mice. (A) Graphical depiction of Rgs10 and Rgs18 genes. Arrows indicate approximate locations targeted by single guide RNAs during CRISPR-Cas9. In both cases, regions within the sequence that encode the RGS domain were targeted. (B) Representative RGS10 and RGS18 immunoblots (IB) (top) of platelet lysates from RGS10+/+18+/+ (denoted “Wild type”) and RGS10−/−18−/− mice with β-actin (bottom) as the loading control. (C) Platelet counts and mean platelet volume of 8-week-old WT, RGS18−/−, RGS10−/−, and RGS10−/−18−/− mice. At least 9 measurements were collected per genotype. NS indicates P > .05; mean ± SEM.