Kujah
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I've typed up a mock method of how to go about doing this. It involves adding different quantities of 5% hydrogen peroxide mixed with distilled water, and uses 1g of fresh liver for each test tube. The result is obtained by measuring the height of the bubbles of oxygen formed when liver and the solution mix, and this gives us an indication of the enzyme activity of catalase.
My question is, how could I improve the design of the experiment?
My question is, how could I improve the design of the experiment?