Figure 5From: A tandem repeats database for bacterial genomes: application to the genotyping of Yersinia pestis and Bacillus anthracisPCR amplification of B. anthracis minisatellite CEB-Bams30 DNA from B. anthracis and B. cereus (six rightmost lanes) was amplified using primers for CEB-Bams30 (Table 2). The PCR products were run on a 40 cm long 2% ordinary agarose gel.Back to article page