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. 2013 Jun;81(6):1964–1973. doi: 10.1128/IAI.00059-13

Table 2.

Primers used in this study

Primer Sequence (5′–3′)a Function Amplicon
1162F CACCATGGGTGCATTTGCGGATGATCC PCR amplification of FlfA flfA
1162R TATTCGTATGCGATAGTATAGTTC PCR amplification of FlfA flfA
FlfA_UF_n2 GGCTCTAGACTCCAAAATGGAGTAGTGAT Deletion mutant generation Upstream fragment of FlfA
FlfA_UR_n2 TATCCCGGGATCTGTTGCAGATTGACAAC Deletion mutant generation Upstream fragment of FlfA
FlfA_DF TTACCCGGGAAGCAAGAAAACAGCCACA Deletion mutant generation Downstream fragment of FlfA
FlfA_DR GGACTCGAGGCTCGGTGAAATGGTTAAT Deletion mutant generation Downstream fragment of FlfA
FlfA_UF2 ACCTTATGTATGCTCCTATG Mutant confirmation
FlfA_DR2 AAAAATCGGGCAGGAAATCT Mutant confirmation
a

The introduced TOPO cloning site (CACC) and start codon (ATG) is indicated in boldface. Introduced restriction sites are underlined.