Abstract
Alkaline phosphatase in the rabbit appendix is almost as well preserved by fixation in chilled acetone as by the freezing drying technic. Acid phosphatase on the other hand is distinctly better preserved by dehydration in the frozen state than after acetone fixation. Acid phosphatase activities are maximal when determined promptly on fresh homogenates. Frozen tissues dehydrated in the frozen state and stored dry at −20°C gave acid phosphatase activities equal to 85% of fresh values and for homogenates stored at 5°C for 24-96 hours the values of fresh and frozen preparations were identical. Acetone and alcohol fixation gave marked reduction in acid phosphatase activity. Alkaline phosphatase activity of fresh tissue is reduced to about 75% of the fresh value by treatment with acetone or absolute alcohol at room temperature. The effects of temperature of fixation, storage in the dry state and embedding in paraffin are noted.