Imagine you have a plasmid and you cut it with three different
restriction enzymes (enzymes 1, 2, 3). You then run these fragments
through a gel and get this separation.
Label the positive and negative terminals on this gel with a
(+) and (-) sign.
If you were working with a single plasmid, how many cut sites
did restriction enzyme 1 have? Explain?
When creating a gel, we stain it with Ethidium Bromide or Gel
Red. What is the purpose...