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. 2011 Jan 24;7:5. doi: 10.1186/1746-6148-7-5

Table 3.

Primers used to amplify the VNTR regions included in the study.

Primer-name Sequence Tm°C Target Optimized Tm° Amplicon size
Fnn-VNTR1F ATCTTGGAAATTAACTACTTTC 46.1 VNTR no 1 55 211
Fnn-VNTR1R ACCTTTTTCTACACCAATAG 47.2
Fnn-VNTR2F GTAAACGTAGTTTTTGGAAGTCCAT 53.7 VNTR no 2 54 217
Fnn-VNTR2R GGATGGCAATCTTGTGTAAA 50.7
Fnn-VNTR3F CAAACCTTCATCTCCACTAC 50.4 VNTR no 3 50 212
Fnn-VNTR3R TGCTCTTTTCCCTCTATATA 47.2
Fnn-VNTR4F AGTTTCATTTATCAGGTGAC 47.5 VNTR no4 54 311
Fnn-VNTR4R AGACTAATAGCCTTCCAAAA 48.5
Fnn-VNTR5F CTGGACATTAGTATCAGGAT 48.3 VNTR no 5 55 312
Fnn-VNTR5R GCAGTGGTAACAATTTTAAG 47.2
Fnn-VNTR6F GCTGTTGGAGATAGTAAATAATTGC 52.3 VNTR no 6 55 301
Fnn-VNTR6R TTAGCTTCTTTAAGACCAAG 47.2
Fnn-VNTR7F CTTCTTCTCAACCATACCAG 50.1 VNTR no 7 54 439
Fnn-VNTR7R ACAAGCATATAGACTTATATTGA 46.9
Fnn-VNTR1-2F AAATGTAGAGTTTCCATCCAAC 47.1 VNTR no 1 55 613
Fnn-VNTR1-2R AGTCGTATTTCTGCTTCAATC 45.6
Fnn-VNTR2-2F CATGGGCTACTTTTGGAATATATAC 47.7 VNTR no 2 55 559
Fnn-VNTR2-2R TCGGTTTGACTGATGTCATG 44.6

Flanking primers were designed based on preliminary data of the whole genome sequence of F. noatunensis ssp. noatunensis isolate GM2212. The attributes of the primers in the study; primer sequence, optimized annealing temperature (Tm°) and amplicon size of the GM2212 isolate.