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. 2001 Jul;45(7):2157–2159. doi: 10.1128/AAC.45.7.2157-2159.2001

TABLE 1.

Oligonucleotide primer sequences for the amplification of the entire ndh genea

Primer Description Sequence Annealing temp (°C) PCR product size (bp)
ndh1S First fragment, sense 5′GCT AAC TGA ACT CGC TCA TC 55 356
ndh1AS First fragment, antisense 5′AAT TCC GAG ACG ACG CAC TG
ndh2S Second fragment, sense 5′GCA ATG TCC AGG TAC TGT TG 57 387
ndh2AS Second fragment, antisense 5′CCT TGG TCG AGT CGA TGT G
ndh3S Third fragment, sense 5′GAC AGA TCG CCG AGC TGG C 60 372
ndh3AS Third fragment, antisense 5′TGG ACA GGT CGG GCA GCA C
ndh4S Fourth fragment, sense 5′GGA CCT TGC CGA GCA ATC AC 60 351
ndh4AS Fourth fragment, antisense 5′CAG GTA CGC CAG GTG CAG CA
ndh5S Fifth fragment, sense 5′CCA AGA TCG GTC CCG TTG AG 59 292
ndh5AS Fifth fragment, antisense 5′ACT GAG TAC CTG GCA GGC TG
a

The M. tuberculosis sequence used to design the primers was obtained from GenBank, accession number Z83859