Bacterial strains, plasmids and oligonucleotide primers used in the current study. Nucleotides in bold represent the restriction enzyme sequence appended to the primers to enable directional cloning in pET28a/pUC18 vector.
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Bacterial strains, plasmids and oligonucleotide primers used in the current study. Nucleotides in bold represent the restriction enzyme sequence appended to the primers to enable directional cloning in pET28a/pUC18 vector.
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2015-12-02



