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. 2011 Dec;77(24):8625–8634. doi: 10.1128/AEM.05155-11

Table 3.

rarA primer sequencesa

PCR amplification site Primer
Locationb Amplicon size (bp)
Forward Reverse
Intact rarA gene ATGAGGGTACTTGTATCCTCC GTTGCAGAAGATATTGGTTTG 1169159–1168918 241
Intact rarA gene + flanking CAATGCTCTCTCGAATAGAAA GTTGCAGAAGATATTGGTTTG 1169460–1168918 542
5′ rarA gene + flanking GATCCTCACATCTTCCTTCTC TCCTTTAGCTGATTTGATGC 1161570–1161092 478
5′ rarA gene ATCTTTTACCGATGCTGTTG TCCTTTAGCTGATTTGATGC 1161282–1161092 190
3′ rarA gene + flanking ACATAATGAATATGGCAGGC CCTTGTGTAAAGTCATTTGTGA 1185696–1185103 593
3′ rarA gene TGGAAGAATAACGTTAATAGCA CCTTGTGTAAAGTCATTTGTGA 1185696–1185458 238
a

rarA primer sequences and characteristics. Sequences for six PCR primer pairs that amplify intact rarA, regions within the 5′ or 3′ split rarA gene, and/or its flanking region. The primer sites within C. botulinum Alaska E43 and the expected amplicon sizes are provided.

b

Location within C. botulinum Alaska E43 (NC_010723.1).