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. 2014 Oct 15;289(49):34349–34365. doi: 10.1074/jbc.M114.587717

TABLE 1.

Primer sequences used in this study

Product Primer name Primer sequencea
ecpA–D ecpAHindIII CCCAAGCTTGTCCTCAATTCAACTCGG
ecpDHindIII CCCAAGCTTGCCGACCGAAATCGCCTG
ecpA–E EcpAXbaI GGACATCACGTCCTCTAGACAACTCGGG
EcpEHindIII TCTGAGGTGGAAAGCTTCCCTCGA
ecpR promoter 0324.5.XbaI GGTCTAGACTTTAATTATGACTC
0324.3.XbaI GGTCTAGATACTTTCCAAACCTG
5′-flanking region of ecpA for deletions 0323.SalI.5F GGAGAGTCGACGAAAAGATTTCGTGTTTATC
0323.NotI.5R CCGTTCCAAGCGGCCGCAAGAGCGTGTATTTCTTCCCGAGTTGAATTG
3′-flanking region of ecpA 0323.NotI.3F CGCTCTTGCGGCCGCTTGGAACGGTCTCTCTGATGTACCAGCAGGG
deletions 0323.PstI.3R GGTGCCTGCAGGGTACTGAAAGTGGTAGTTTG
3′-flanking region of ecpD for deletions 0320.Not1.3F CGCTCTTGCGGCCGCTTGGAACGG TAAGGCCCTGCTGACAGCGGTCTG
0320.PstI.3R TTAATCTGCAGCTTAAACCACGTGTTGCCGGTG
ΔecpA.NotI linker 0323.SalI.5F For splice overlap extension PCR of products ecpA.5.Not and ecpA.3.Not PCR products
0323.PstI.3R
ΔecpA–D.NotI linker 0323.SalI.5F For splice overlap extension PCR of products ecpA.5.Not and ecpD.3.Not PCR products
0320.PstI.3R

a Restriction enzyme sequences are underlined.