Figure 3
Figure 3. H2ax−/−p53−/−Rag2−/− mice develop thymic lymphomas with p53 inactivation. (A) Schematic of the p53+ allele. The relative locations of where the 11 exons of p53 are located within the 20-kb EcoRI genomic fragment. The location of the 400-bp AvaI (A) and the p53 last exon (B) probes used for Southern blotting are indicated by black rectangles. (B) Southern blot analysis of EcoRI-digested genomic DNA isolated from 6 H2ax−/−p53−/−Rag2−/− thymic lymphomas and a p53−/− mouse-tail probed with either probe A or B. The fragments corresponding to the p53+ alleles are indicated. (C) Western blot analysis of protein isolated from 4 H2ax−/−p53−/−Rag2−/− thymic lymphomas and p53−/− or p53−/− control cells using either an anti-p53 antibody or an anti-H4 histone antibody as a loading control.

H2ax−/−p53−/−Rag2−/− mice develop thymic lymphomas with p53 inactivation. (A) Schematic of the p53+ allele. The relative locations of where the 11 exons of p53 are located within the 20-kb EcoRI genomic fragment. The location of the 400-bp AvaI (A) and the p53 last exon (B) probes used for Southern blotting are indicated by black rectangles. (B) Southern blot analysis of EcoRI-digested genomic DNA isolated from 6 H2ax−/−p53−/−Rag2−/− thymic lymphomas and a p53−/− mouse-tail probed with either probe A or B. The fragments corresponding to the p53+ alleles are indicated. (C) Western blot analysis of protein isolated from 4 H2ax−/−p53−/−Rag2−/− thymic lymphomas and p53−/− or p53−/− control cells using either an anti-p53 antibody or an anti-H4 histone antibody as a loading control.

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