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. 2012 Mar 7;7(3):e32702. doi: 10.1371/journal.pone.0032702

Table 2. Synthetic oligonucleotides used in this study.

Sequence* Restriction sites Binding region
B5fw TATAGGCGCCGAATTC ATGACTGAATCTTTTGCTC NarI, EcoRI, rpsA from codon 1
D5fw TATAGGCGCCGAATTC ATGAAAGCTAAACGTCAC NarI, EcoRI, rpsA from codon 87
G5rev TATACTCGAGTTATTTTTCATCGTCATCCTTATAGTCAGCATCTTCGTAAGC XhoI rpsA until codon 106
H5rev TATACTCGAGTTATTTTTCATCGTCATCCTTATAGTCCATGCCTTCCTGCAGGGTCCATGCCTTCCTGCAGG XhoI rpsA until codon 194
I5rev TATACTCGAGTTATTTTTCATCGTCATCCTTATAGTCGCCTTTAGCTGCTTTG XhoI rpsA until codon 557
V14fw [P]GCCGTTATCGAATCCGAAAAC rpsA from codon 182
W14rev [P]GTAAGCTTTTTCCAGCGTGATCC rpsA until codon 102
J5 TATAGAATTCCTCGAG GGTCTGTTTCCTGTG EcoRI, XhoI pProEX-Htb specific primer used for site-directed mutagenesis
H4fw TATACATATG AACCATCGCTGGCTGG NdeI rpsB from codon 93
I4rev TATACTCGAG TTAGTCCGGCAGACCGC XhoI rpsB until codon 159
*

Restriction sites are highlighted in italics; sequences encoding the FLAG-tag are shown in bold, and sequences complementary to the template are underlined.