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. 2015 Jul 10;10(7):e0132431. doi: 10.1371/journal.pone.0132431

Table 1. Primers used in this study.

Name a Sequences (5’-3’) PCR products
med12-L1 5’-CCCAAGCTTGGTATCGGCACCTCTTC (HindIII) 1.5 kb DNA located in the upstream of med-ORF12
med12-L1 5’-GCTCTAGA CATCGTTTTCG TTCTCCCG (XbaI)
med12-R2 5’-GCTCTAGA TGAGGGCGCCGTGCGGTC (XbaI) 1.3 kb DNA located in the downstream of med-ORF12
med12-R2 5’-GGAATTCAAGCTTGCGGACCAGAACCAG (EcoRI-HindIII)
med12-qc1 5’-CCGTCCTCCGTGGTGATCTCGAAG 1.7 kb/0.5 kb fragment (wild type/mutant) flanking upstream and downstream of med-ORF12
med12-qc2 5’-GTTGACGACGAACTCGGACGCGGC
med12-A 5’-GGAATTCCATATGAGCGGAACCGGCCGGCC (EcoRI- NdeI) 0.975 kb full-length med-ORF12
med12-B 5’-CGGGATCC TCACGACGCGCTCCC GGGCT (BamHI)

Note:

a: Sequences underlined in the primers were recognition sites for restriction enzymes indicated in parentheses. Start/stop codons (ATG/TGA) were shown in bold.