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. 2008 May 23;190(15):5394–5403. doi: 10.1128/JB.00488-08

TABLE 2.

Primers used in this study

Primer Sequence (5′ → 3′)a Application
narK2F GACACGATCCGGGGTCTCG Reporter assay, gel shift assay, DNase I footprinting
narK2R TCCCCTTTCCAGTGGCGACC Reporter assay, gel shift assay, DNase I footprinting
narK2F1 GGGGAATTCCGGACAGCCATGCGCTAACCC Reporter assay
narK2R1 GGGGAATTCCCCTCCGATAGGGCCTGAAGT Reporter assay
narK2R3 GTTCCACGCCCAGAAGTTGAC Primer extension
Rv1738R CGCCCGAGTCAATCCTTCGTGTTC Primer extension
PD1 ATGGCGCCGGCTCAGTTACCCCCGGAAGTCCCC Mutational analysis
PD2 CACTGCCCTGATTCGTCCGCCAGGGGC Mutational analysis
PD3 AGCCCTCCGATAGGGCCTGAAGTGGGGGCCACTGGGGTC Mutational analysis
a

EcoR1 sites are underlined, and mutated residues are in boldface.