Skip to main content
. 2013 May;195(10):2177–2186. doi: 10.1128/JB.00035-13

Table 2.

Oligonucleotide primers used in this study

Primer Sequence (5′–3′)a Restriction site Description and target gene
1848 CTCTACGGGCCCACTTCTGTCTCCCCACTGG ApaI Up-for, Δagl16
1849 AAGGTCTGGATGTTGTAAAAATTATGTCCATGACATCACAGGACA Up-rev, Δagl16
1850 TGGACATAATTTTTACAACATCCAGACCTTATACATGAATCATCC Down-for, Δagl16
1851 CGCCGAGGATCCAACCATGGAATTGTAGCC BamHI Down-rev, Δagl16
4101 GTCCTCAAGACCCAATTCACTAAC RT-PCR-for, agl16
4106 GCCGACTGCAGCATTAGTAATGACTCCACACCAC RT-PCR-rev, agl16
2799 CATGCGGATCCTTAACTTAAACTTTTATAGAGCTCAAGC BamHI Forward primer complementing agl16
4100 CATGCCCATGGATGTATAAGGTCTGGATGTTGACCCCAC NcoI Reverse primer complementing agl16
1729 CTGCTGCAATTACAGCGTTC RT-PCR-for aglB
1730 AACCGTGAGCTACTTCAGAC RT-PCR-rev aglB
a

Underlining indicates restriction sites.