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. 2017 Mar 30;6(4):e00468. doi: 10.1002/mbo3.468

Table 4.

Primers designed for qRT‐PCR

Gene Primer sequence (5′ → 3′)
acuC Ac‐F AGGACGATGCCTACCTCACC
Ac‐R GCGTTTGTTCGCCTCTTCA
cblA Ad‐F CCGAGGCGTTCTATGTGCA
Ad‐R TTGGTCAGGTAGCCGGTGAT
aerA Ae‐F GGTCTGTGGCGACAAGTATCG
Ae‐R AGAGCAGACAGAGTCGGTATTTCTC
ascV As‐F GGGTATTCACCTGCGTTTCA
As‐R GATGTTCATTAGCGACCCACA
hlyA Hl‐F CCGCCCAGTCCTTCATCTAT
Hl‐R AGGGTCCGTAGGCTCACATT
ompA Om‐F CTCACGATCTGGGTGACTTTG
Om‐R CGCCGTTGATGGACTTGA
ompTS Pr‐F AATGGCTCCTTCCCTGATCG
Pr‐R TGGCACCCTGGTTCTCGTAA
vash Va‐F AAACTGGCACGGGGAAAGAG
Va‐R GCTTGTAAGGTGAGCGGCATAT
traA Tr‐F GTGATGGTCGTCGCCTTTCT
Tr‐R GATAACCTTCTCCGCATTTTCC
pilB Pi‐F CTAATGCGAATGCAGCACGTA
Pi‐R CGCTTCAACAGTTCCAACCA
rfaf Rf‐F TACCTGGCACTGGCCTATCC
Rf‐R CTCGTCGAGGTGCTTTTGTG
degQ De‐F CACCGAGCTTACCTCCGAAAT
De‐R CCGCCTTCTTCAGCGTGAC
flgE Fe‐F CCCGCTCAGACATTGGAGAT
Fe‐R GTCGCATTGCTGTAGGTCGC
flgL Fl‐F GCCCCAGAACAACAACATCC
Fl‐R GCCGCATCCTCTTTTGACA
16s 16s‐F GGGGAGTACGGTCGCAAGAT
16s‐R CGCTGGCAAACAAGGATAAGG