If extra copy of restriction site need to be added for digestion of a vector with Bsa1, how such oligos are designed ?.....What should be the sequence composition ? Could anyone please help me to clarity this ?
I'm not entirely understanding your question. But if you have a plasmid that carries a BsaI site, then it should digest fine without adding any oligos.
Or are you talking about adding a second BsaI site to a plasmid?