Fig. 1.

Genotyping and verification of the iPLA₂β^−/− model. DNA was generated from tail clips and progeny were genotyped by PCR analyses. Reactions were performed in the presence of primers for the WT sequence (sets 1 and 2) or for the disrupted KO sequence (sets 3 and 4) for each mouse. The expected bands for WT (1,400 bp) and KO (400 bp) in two mice each are presented.