The process of genetic modification involves:
1. Isolation of the desired gene (e.g., the gene for insulin)
2. Cutting the gene using restriction enzymes
3. Cutting a bacterial plasmid using the same restriction enzymes
4. Joining the human gene with the cut plasmid DNA using DNA ligase to create a recombinant plasmid
5. Inserting the recombinant plasmid into bacteria
6. Allowing the bacteria to multiply, carrying the modified genetic material
7. Bacteria using the inserted human gene to produce the desired protein (e.g., insulin)