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