I have my gene of interest cloned in mammalian expression system. there are two gene that i am looking for. i have cloned each of them in two different plasmids both having different promotors of nearly similar strengths with differnt aantiobiotic resistant genes. i wish to generate a stable cell line for each of these plasmids. what should be the range of concentraion of antibiotic (puromycin and neomycin) used for generting a stable cell line?