Overview
This protocol exploits the discovery that RNase A can efficiently cleave at single rC or rU bases embedded in double-stranded DNA. Entire plasmid vectors are amplified using long, high-fidelity PCR with riboprimers, which carry a single rC residue at their 3' end. By Wayne M. Barnes.
Details
Details of this protocol, Ribocloning: DNA Cloning And Gene Construction Using PCR Primers Terminated With A Ribonucleotide (Subscription Required), are located on a web site other than Biocompare Protocols.