This program follows the procedures for placing DNA in a well at one end of an electrophoresis gel: heating the gel and containing it when molten, leaving it to set, loading the digested DNA samples together with loading buffer, and switching on the power. At this point, electrophoresis begins. While it is taking place, the movement of DNA can be monitored. The program explains the function of ethidium bromide and the process of intercalation. Finally, when the transilluminator is turned on, the DNA samples can be seen glowing strongly. (14 minutes)
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