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. 2016 Aug 26;291(42):22315–22326. doi: 10.1074/jbc.M116.744532

TABLE 3.

PCR primers used to screen for deletions at the indicated loci

AES, allelic exchange substrate.

Locus Flank Primer name Binding site Primer sequence
Rv1151c Left 1151c L Flank F = P7 Upstream of L flank, in wild-type and mutant CAT GCC GTT CAG CAT GTC
sacBout_LR = P10 Within AES construct, mutant only GAT GTC TCA CTG AGG TCT CT
1151c L Flank R = P8 Within deleted region, wild-type only GGT GAT GAC GCT GAC CTC
Right 1151c R Flank F = P5 Within deleted region, wild-type only CGT CAT CAC CCA GAA TGT C
hygout_RR = P9 Within AES construct, mutant only CGA GTG TCT GGT CTC GTA G
1151c R Flank R = P6 Downstream of R flank, in wild-type and mutant GGC ACT GTC GGA TTA CAA G
Rv0998 Left 0998 L Flank F = P1 Upstream of L flank, in wild-type and mutant CGT TGT GTC TAC TGC TCG AC
sacBout_LR = P9 Within AES construct, mutant only GAT GTC TCA CTG AGG TCT CT
0998 L Flank R = P2 Within deleted region, wild-type only GAT GAT CGC AAC ACC ATC
Right 0998 R Flank F = P3 Within deleted region, wild-type only CGG TTC ATG TCG GCT CGT GTT C
hygout_RR = P10 Within AES construct, mutant only CGA GTG TCT GGT CTC GTA G
0998 R Flank R = P4 Downstream of R flank, in wild-type and mutant TGT GCG GTA CAT CGA CCA CCT C