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. 2012 Dec;50(12):3831–3837. doi: 10.1128/JCM.01893-12

TABLE 1.

PCR amplification primers used for full-length Ion Torrent analysis of M. tuberculosis genes

Amplification target Forward primer Reverse primer Amplicon length (bp)
rpoB 5′-TCCTCTAAGGGCTCTCGTT-3′ (19 nta) 5′-GTCAGGTACACGATCTCGT-3′ (19 nt) 1,625
rpoBII (second half) 5′-ATCGAAACGCCGTACCGCAA-3′ (20 nt) 5′-TGACGTCGAGCACGTAACTCCCT-3′ (23 nt) 2,056
katG 5′-ACACCAACTCCTGGGAAGGAAT-3′ (21 nt) 5′-TGATCGCACATCCAGCACATTT-3′ (22 nt) 2,447
pncA 5′-GACGGATTTGTCGCTCACTAC-3′ (21 nt) 5′-GCCGGAGACGATATCCAGAT-3′ (20 nt) 960
gyrA 5′-AAGGATGTTCGGTTCCTGGAT-3′ (21 nt) 5′-TAACACTCGTACCCGGCT-3′ (18 nt) 2,664
rrs (16S) 5′-TTCTAAATACCTTTGGCTCCCT-3′ (22 nt) 5′-TGGCCAACTTTGTTGTCATGCA-3′ (22 nt) 1,680
Total 11,432 total (5 genes)
a

nt, nucleotides.