Hello coleagues!
I´m planning some experiments for blaKPC cloning in pCR-Blunt II TOPO. The aim of these experiments is to proof that MIC of certain antibiotics in the parental strain are due to blaKPC gene (or not), therefore I need the protein to be expressed once cloned in the vector. As the vector has plac (lactose promoter), I understand I can express my protein by inducing plac with IPTG, but do you know if I would need to add IPTG on culture media not only for transformant selection but also when I am testing MIC of the antibiotics? MANY THANKSS IN ADVANCE