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Using recombinant and , cloned under different promoters, confirmed their TA nature, as expression was able to reverse growth inhibition by CptA in a dose-time dependent manner. Furthermore, transcriptional analysis of in clinical and standard strains demonstrated the downregulation of this system under oxidative and antibiotic stress. Combining in silico and studies confirmed the predicted TA nature of a -like system in . Transcriptional analysis suggests a possible role of in response to antibiotics and stress factors in , making it a
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