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. 2009 May 11;77(7):2832–2839. doi: 10.1128/IAI.01218-08

TABLE 2.

Primers used in this study

Locusa or primer name Sequence (5′-3′)a
Use
Forward Reverse
ers CGCGGATCCATAATAGATAATTGAGG TTGCTGCATCTTTTTCATGG RT-qPCR
ef0082 TTGACGTCAGCACCTTCTTC CGTAGCGTTCACCTTTGACA RT-qPCR
ef0049 CAGCTTTTCCGACACGTCTT TTCCCCCACGTACTTTAGCA RT-qPCR
ef0782 TTAGAGCGCGCAGTGAATC ATGGCCGATCTGCTTCTAAA RT-qPCR
ace ATGAAGGAAGCCCACAGTTG GTTGTGCCTGTTTTGGGAAG RT-qPCR
kat GCTGTTTGGGATTTTTGGTC CATGCATATGACGGAACGAC RT-qPCR
ef1656 TTTATTTGTCACCCAACCAACA CAATTGAAACGGTTGATCAGAA RT-qPCR
ef1664 TGGCGACCTAATTACCTTGG CGTTTGCATCGTACGTGAGT RT-qPCR
ef1816 CGTCAAGACGATACCCGATT TTTCCATGTTGTGCAGGAAG RT-qPCR
ef2185 GCGATTGCTCCAACTGAATC GCCGTCCGTAATAAAAAGCA RT-qPCR
ef3146 CCAGAATTCTCAATTCCTCGTT CAAATTTTTGTACACCGACAGG RT-qPCR
aceRace1 ATTCCAACTAGTGCGTCTGG 5′RACE PCR
aceRace2 TTGAGGTCATCTCTCCTTG 5′RACE PCR
aceRace3 TCAATTCGGCGCCAAACGAA 5′RACE PCR
Prom-ace TCATTCTTTTCCTCCTTATCT CCGCAATTGGTAGAATCATTA Cloning in pGEM-T
Prom-ers TAAGTTTGGTTCTGTCATTA CGACTCGAAAGGAATGTTCA Cloning in pGEM-T
aceDC-Ub CCGGAATTCAGCTCAACTATGCCTGTCGA CGCGGATCCGTCATTCCAACTAGTGCGTC Cloning in pMAD
aceDC-Db CGCGGATCCCAGCCATCCACAGAAACAAC GAAGATCTTTCCTCTGCCATTAACGCGT Cloning in pMAD
p3535ers CGCGGATCCATAATAGATAATTGAGGAGTTA CGCGCGCTGCAGTTAAACAATAATGTTATCTCTAATC Cloning in pMSP35535
pQE30-ersHTH GCGGATCCAAAAAGATGCAGCAAATGTTGAT CGCGCGCTGCAGTTAAACAATAATGTTATCTCTAATC Cloning in pQE30
mad1F TCTAGCTAATGTTACGTTACAC Cloning verification
mad2R TCATAATGGGGAAGGCCATC Cloning verification
Pu GTTGTAAAACGACGGCCAGT Cloning verification
Pr CACAGGAAACAGATATGACC Cloning verification
a

From the annotated sequence available at http://www.tigr.org.

b

Primers used to clone upstream (U) and downstream (D) sequences of ace in order to construct a deletion mutant and complemented strain by a double-crossover (DC) event.

HHS Vulnerability Disclosure