1. Isolate the desire gene from the original species using restriction endonuclease (If the gene is eukaryotic, use reverse transcriptase to produce an edited version of the gene)
2. Isolate an appropriate vector (used to deliver DNA fragments into a cell) in this case, a plasmid
3. Cut plasmid with restriction endonuclease--> opens the loop, turning it into a string
4. Sticky ends are left by the enzyme, or it can be made by adding nucleotides
5. Mix the cut plasmids and target DNA
6. DNA ligase makes sugar-phosphate bonds between plasmid and DNA
7. Transfer the recombinant plasmid into the bacterium