I started my day off by practicing loading dye into 96 well dishes for later this morning. Then I counted some cells. Later on I went with the lab tech to make another Pulse/Field Gel Electophorisis. After we got the gel we then put it in a kdjfka bromine to stain the DNA so that its picture could be taken. Then I went to the lab to fill the four plates from yesterday with dye so that we could see how different concentrations of the drug could would effect its color change. A few minutes later we went to another lab to use the Typhoon, the machine used to take the gel's picture. Then later in the afternoon we put the 96 well dishes in a plate reader to measure each of the four plates' optical density. Then I ended the day by finishing counting the cells.