Hello everyone, this is my first post and I am hoping it is the right place to ask.
I just recently started cloning, PCR design and similar. I have very basic question and would like to get an answer step by step if possible, using an example ππ»
So I have a pool of oligos (with short stretch of the same sequence at 5β and 3β so I can do PCR with it, for example to introduce nuclease sites). My question is, how do I design a primer for PCR to introduce biotin site and letβs say one of any restriction enzymes??
I hope I provided enough of info, I need only one primer.
thanks a lot!!! π€