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. 2009 Feb 17;77(5):1842–1853. doi: 10.1128/IAI.01216-08

TABLE 1.

Oligonucleotides used in this study

Primer Sequencea Restriction enzyme site
Hfq-1 attcagaattcGGTTTCCGTGCGGGTGGTAAGGC EcoRI
Hfq-2 GCTAAAGGACAAATGTTGCAggatccGCACGAAGCATGACGTGTC BamHI
Hfq-3 GACACGTGATGCTTCGTGCggatccTGCAACATTTGTCCTTTAGC BamHI
Hfq-4 attcagaagcttACGCGAAGCAGGCAGGTCTATGG HindIII
Hfq-F attcagcatATGACAGCTAAAGGACAAATGTTGCAAG NdeI
Hfq-R attcagctcgagTTATTCGGCAGGCTGCTGGACGGTTTCC XhoI
Hfq-R-Ns attcagatgcatTTATTCGGCAGGCTGCTGGACGGTTTCC NsiI
Hfq-S1 CTCAGGAGAACAACGTATTGATCG
Hfq-S2 GTTACCATCGTATTGCTGAAtTCGCCCACATC EcoRI
0747-F GAAAGTGTGGGCATTCGAC
0747-R TTGCTGTAACCTGCTTCCTG
16S_F ACGGAGGGTGCGAGCGTTAATC
16S_R CTGCCTTCGCCTTCGGTATTCCT
a

Capital letters in roman type indicate N. meningitidis-derived sequences, capital letters in italics indicate E. coli-derived sequences, lowercase letters indicate sequences added for cloning purposes, and underlining indicates recognition sites.