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How is the second strand built on using the copied DNA as a template?

What does this produce and what are added?

How are the plasmids cut open and what are they mixed with?

What happens if a plasmid takes up the gene?

What then happens to these plasmids?

Where is the bacteria placed?

What are the 3 possible types of colony that may grow?

What is the modern process used to identify transformed bacteria?

What are chosen as the genetic markers?

What is susceptible to both of the antibiotic chemicals?