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. 2016 Jan 22;82(3):939–953. doi: 10.1128/AEM.03741-15

TABLE 4.

Oligonucleotides used for qRT-PCR experimentsa

Primer Oligonucleotide sequence (5′-3′) Product size (bp) Primer efficiency (%)
16S rRNA-Fb TTA GCT AGT TGG TAG GGT 318 91.3
16S rRNA-Rb AAT CCG GAC AAC GCT TGC
emrE-JKq-F GTT GCT ATA GCG GTG ATT GGA GT 102 104.3
emrE-JKq-R GTT CAG GCC TAC AAC CCC TG
lde-JKq-F TCC CAA TGG CTT TCG CAC AA 136 99.4
lde-JKq-R ATT CGA CCT GCA ACC TCA CG
lmo1861-JKq-F GCT TAC AGA AGA AGG AGC GCA 101 99.6
lmo1861-JKq-R CCC TAC GTT GTT CCT GCG G
mdrL-JK2q-F TCG AGC TGG TTG GGG TTT TG 96 97.1
mdrL-JK2q-R ATC CCA ATT GCA TGG CCT GG
sigBq-Fc TGT TGG TGG TAC GGA TG 221 100
sigBq-Rc CAT TCT GCA ACG CCT C
a

All primers were synthesized by Integrated DNA Technologies, Inc. (Coralville, IA).

b

Primers validated by Tasara and Stephan (38).

c

Primers designed by Arguedas-Villa et al. (19).