Hello,everyone.I want to introduce EcoR1 and Not1 sites into the original Xba1 site in PGL3 vector.How can I do that?Are there some references about that?
PGL3 should not be too big. You can design a pair of primer with your EcoRI and NotI and PCR the whole plasmid out and transform into E. coli. Usually I can get more than 90% colonies with the right sites in. Go to check NEB website for details: