Microscopy Procedure
To start the lab, we labeled five test tubes from zero to 40 minutes, and one with the label of Tet+Ink. Next, 500 microliters of Tetrahymena solution was and another 500 microliters of India Ink was added to the tube labeled Tet+Ink. We had to add seven microliters of serotonin to the same tube to assess how the serotonin would affect the rate of phagocytosis in the tetrahymena cells. In the five other tubes labeled from zero to 40 minutes, we added 20 microliters of glutaraldehyde solution (WE DID NOT add glutaraldehyde to the Tet+Ink tube). After starting a timer we immediately added 100 microliters of the solution in the Tet+Ink tube to the first tube, labeled zero minutes. At ten minute intervals, 100 microliters of the Tet+Ink solution was added to the next tubes. We were careful to mix the solution and glutaraldehyde within the tubes. After 40 minutes passed, we put 15 microliters of the solution in each tube onto separate microscope slides. We then observed and counted the number of dark colored vacuoles in ten different cells for each slide. Finally, we recorded the number of vacuoles found into a table and calculated the average and standard deviation for each tube.
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