This lab requires three main materials, the dyed agarose gel, DNA from each virus, and an electric chamber. The agarose gel will be dyed in order to show the visual effect while in the electric chamber connected to the positive (red cord) and negative (black cord). The chamber is filled with Tris/Borate/EDTA (TBE) buffer solution since the agarose gel is compatible with the buffer solution. The DNA strands will be held in tube samples in the amount of two tubes dedicated to each virus. The DNA will be inserted into an agarose gel using disposable plastic needle-nose micropipette. Each tube has an assigned plastic needle that will be switch during transitions to a new tube, this allows no cross contamination to occur. Once the gel
