We have a layout .. and our information that we conduct during our lab goes unerneath our "Materials and Methods" or the "Results"..
Answer:
Cut open the plasmid and "paste" in the gene. This process relies on restriction enzymes (which cut DNA) and DNA ligase (which joins DNA).
Insert the plasmid into bacteria. Use antibiotic selection to identify the bacteria that took up the plasmid.
Grow up lots of plasmid-carrying bacteria and use them as "factories" to make the protein. Harvest the protein from the bacteria and purify it.
Explanation:
<span>1) regulation of enzyme activity. 2) regulation of enzyme production.</span>