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. 2017 Dec 8;39(2):242–251. doi: 10.1093/carcin/bgx137

Figure 1.

Figure 1.

Generation of ARH1 and CD38 double-knockout mice. (A) Genotyping of mice. ARH1 primers amplified a 0.8-kb fragment from the wild-type allele and a 1.0-kb fragment from the knockout allele (solid arrow). CD38 primers amplified a 0.4-kb fragment from the wildtype allele and a 0.5-kb fragment from the knockout allele (dotted arrow). Two mice were used for each genotype. (B) CD38 expression by splenocytes from wild-type, ARH1−/−, CD38−/− and ARH1−/−/CD38−/− mice as assessed by flow cytometry. Data are representative of two independent experiments and are shown as histograms with an overlay of CD38 expression by wild-type splenocytes (gray peak). (C) ARH1 expression in mouse brain lysates detected by Western blot (n = 3).