Lab 9 entry

Once my DNA was extracted, I prepped it for gel electrophoresis.

  1. First, we dotted ~2mL of blue tracking dye on a piece of parafilm.
  2. Then, I put ~3mL of each extracted DNA on top of a dot, changing tips every time.
  3. Finally, I put my pipette on 6mL and moved the solution from the parafilm into the wells of the gel.
  4. We ran the gel. 


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