Today, Cohen is a professor of genetics and medicine at Stanford, where he works on a variety of scientific problems including cell growth and development.
Stanley Cohen, Paul Berg and Herbert Boyer made what would be one of the first genetic engineering experiments, in 1973. They demonstrated that the gene for frogribosomalRNA could be transferred into bacterial cells and expressed by them. First they developed a chemical cell transformation method for Escherichia coli,[5] then they constructed a plasmid, which would be the vector, called pSC101.[6] This plasmid contained a single site for the restriction enzymeEcoRI and a gene for tetracycline resistance. The restriction enzyme EcoRI was used to cut the frog DNA into small segments. Next, the frog DNA fragments were combined with the plasmid, which had also been cleaved with EcoRI. The sticky ends of the DNA segments aligned themselves and were afterwards joined together using DNA ligase. The plasmids were then transferred into a strain of E. coli and plated onto a growth medium containing tetracycline. The cells that incorporated the plasmid carrying the tetracycline resistance gene grew and formed a colony of bacteria. Some of these colonies consisted of cells that carried the frog ribosomal RNA gene. The scientists then tested the colonies that formed after growth for the presence of frog ribosomal RNA. (Thieman, W.J and Palladino, M.A., Introduction to Biotechnology, Pearson Education, Benjamin Cummings, 2024. page 55)