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5 Cards in this Set

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  • Back

1.

DNA samples are treated with restriction enzymes to cut them into fragments.

2.

DNA fragments are placed into wells cut into one end of the agarose gel.

3.

The gel is immersed in a buffer solution and an electric current is passed through the solution for two hours.

4.

DNA, being negatively charged, diffuses through the gel towards the anode (positive electrode).

5.

The position of the DNA fragments is shown using a UV sensitive dye, radioactive marker or photographic film.