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. 2008 Mar 12;105(11):4247–4252. doi: 10.1073/pnas.0800276105

Fig. 1.

Fig. 1.

The generation of Mlh1G67R mutant mice. (a) Domain structure of Mlh1. The location of the G67R mutation is indicated. (b) Schematic representation of the modified Mlh1G67R genomic locus and sequence characteristics of the G67R mutation. (c) PCR genotyping of tail DNA from Mlh1G67R mutant mice. Mlh1G67R/+, heterozygous mice; Mlh1G67R/G67R, homozygous mutant mice. After EcoRI restriction digestion of the PCR product, the WT allele is indicated by an 880-bp fragment and the Mlh1G67R mutant allele by 470- and 410-bp restriction fragments. (d) Western blot analyses of thymocyte cell extracts using anti-Mlh1 and anti-Msh2 antibodies.*, Unspecific protein recognized by the Mlh1 antisera.