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. 2018 Jan 26;13(1):e0191286. doi: 10.1371/journal.pone.0191286

Table 1. Primers used to amplify and clone APP III gene sequences and E. coli ClyA sequences.

Gene Primer sequences (5’-3’)
ClyA-F CGCCGAGCTCATGACTGAAATCGTTGCAGATA
ClyA-R TGCTCTAGAGACTTCAGGTACCTCAAAGAGTG
ApxIAr-F TGCTCTAGATATGCGGGTAACGGACATGATG
ApxIAr-R ACGCGTCGACAATATCCTTACCTAAACCACCGTAG
ApxIIAr-F ACGCGTCGACAATTTAGGTGCTGGTAACGATAATG
ApxIIAr-R TGCCAGTTTATCTTGTCCGC
ApxIIIAr-F CTCTGGCGGACAAGATAAACTGGCACATCTAGGCAATGGTAATGA
ApxIIIAr-R CCCCAAGCTTTTAGTGGTGGTGGTGGTGGTGAAAATCGCTACCATCGCCTCCT

The underline portions of the primer sequences were the restriction enzyme cutting sites (ClyA-F (forward): SacI; ClyA-R (reverse): XbaI; ApxIAr-F: XbaI; ApxIAr-R: SalI; ApxIIAr-F: SalI; ApxIIIAr-R: HindIII).