1) What is genetic transformation?
2) which plate should have no growth and why?
3) what did our plasmid carry?
4) why did a plate contain arabinose?
5) why did we add LB broth?
6) what does CaCl2 do?
7) why did we heat shock the bacteria?
8) what does sodium citrate do?
9) what does SDS do?
10) why did we add alcohol to the tube for extraction?
11) what is the wild-type color of the colonies? what is the transformed color?