Genetic Modification using Bacterial Production of a Human Protein
1. Locate gene to be inserted
2. Use restriction enzymes to isolate gene with 'sticky ends'
3. Cut bacterial plasmid with same restriction enzyme
4. Use DNA ligase to join gene and plasmid
5. Insert engineered plasmid into bacterial cell
6. Bacteria reproduce, copying plasmid and expressing gene
7. Genetically engineered bacteria placed in fermenter to rapidly reproduce and produce human protein