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. 2010 Sep 11;52(1):52. doi: 10.1186/1751-0147-52-52

Table 1.

Primers, sequences and PCR conditions used for the amplification of apxIA, apxIIA, apxIIIA, apxIVA, omp and apfa from Actinobacillus pleuropneumoniae

Genes Primer sequences (5'-3') Annealing
temperature
Size of PCR
product (bp)
apxIA Forward: GCGGGATCCAACTCTCAGCTCGATAG 55°C 2520
Reverse: GATGCGTCGACAGCAGATTGTGTTAAAT
apxIIA Forward: GCGGGATCCATGTCAAAAATCACTT 54°C 2721
Reverse: GCGAATTCAGCGGCTCTAGCTAAT
apxIIIA Forward: ACGGGATCCTGGTCAAGCATGTTAG 52°C 3114
Reverse: ATGCGTCGACTGCTCTAGCTAGGTTACC
apxIVA Forward: GCCGAATTCCGCGCCTATATCTGG 54°C 2553
Reverse: ATGCGTCGACCCCTTCGAATTGTTTC
Omp Forward: GGAATTCACGCCTAAGGTTGATAT 53°C 984
Reverse: GGTCGACCTTTATCTTCTTTTGTTG
Apfa Forward: GGGCGAATTCATGCAAAAACTAAGT 53°C 444
Reverse: TATGGTCGACTGATGCGCAGAAAT

Note:

BamH I site: Underlined; EcoR I site: Italic; SaI I site: Bold; PCRs were run for 30 cycles.