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.