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. 2008 Jun 20;40(3):339–344. doi: 10.3858/emm.2008.40.3.339

Figure 1.

Figure 1

T-cell specific disruption of BRCA2 using Cre-loxP recombination system. (A) Schematic representation of wild type and mutated BRCA2 alleles. Two loxP sites as triangle flanks exon 11 of BRCA2 (BRCA2F11). Recombination by Cre recombinase can induce excision of exon 11 (BRCA2Del11). Small arrows indicate PCR primer sites for mouse genotyping. (B) General genotyping pattern using PCR screening. Using primer 10F and 10R in Figure 1A, wild-type allele is represented as 298 bp band, but band of BRCA2F11 is shifted to 376bp, since additional loxP sequences add up.