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. 2010 Dec 17;193(4):909–917. doi: 10.1128/JB.01175-10

TABLE 2.

Primer sequences

Use Primer Sequence
DNA contamination rplU-for CGCAGTGATTGTTACCGGTG
rplu-rev AGGCCTGAATGCCGGTGATC
RT-PCR 57RT′+ CGGCGGTCGGCGATTCCCTC
58RT′− CAGCGAGCGGCGGCAGTAATC
58RT+ CCTGGCCGAAGCCTCGCAACG
59RT− GCGAATCCTCGGCATTCACCAG
59RT+ GGAGCGCTATCGCTGCTG
60RT− GTGTCGAGGCCGACGTGCAGC
60RT+ GCTGCGACTGATCGCCCAGAC
61RT− GCACCGAGATCATCACCAGG
EMSA probes 57promF-XbaI GCTCTAGAGAGAGGTTCCGATGCGGATTG
57promR-EcoRI GGAATTCCGCAAGACCAGCAACAACTAC
PA3757intF GCTGCCCTCCGAACGCAACC
PA3757intR CCGTCCAGGTATTCGTAGAGG
nagA flanking region 57F-P1 GGAATTCGAAGACAGCCCACGACCTGC
57R-P1 CGGGTGACTTTGCTCAGGTGCCGTGTCGGTTCAGCGTCGCAG
glmS flanking region 60F-P2 CGTGTCGGTTCAGCGTCGCAGGCACCTGAGCAAAGTCACCCG
60R-P2 GGGGTACCCGCCGAGGGCCGCCTCGCTGTC
Plasmid constructs 61-FcompEcoRI GGAATTCGCAACACTGGCCGCTGGCCTG
61-RcompHindIII CCCAAGCTTGTAGGGCGGATAACCGCTTGG
57promF-XbaI GCTCTAGAGAGAGGTTCCGATGCGGATTG
57promR-EcoRI GGAATTCCGCAAGACCAGCAACAACTAC
NdeIPA14_15830F GGAATTCCATATGAAGACAGCCCACG
3′N-57NdeI GGAATTCCATATGTCAGCGTCGCAGT