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Triton X-155 as a Stabilizer of Bovine Plasma Arylesterase Activity^{1, 2,}

Department of Animal Sciences, Washington State University, Pullman

ABSTRACT

Efforts to purify bovine plasma arylesterase were severely handicapped by 1) lack of agreement between duplicate assays and 2) rapid loss in enzyme activity of dilute, partially purified preparations. These difficulties were overcome by the inclusion of Triton X-155 (0.25%) in the reaction mixtures during assay and in buffer solutions (0.01% or more) containing the enzyme.

¹ College of Agriculture Scientific Paper no. 2896. Work conducted under Project 1597. This investigation was supported in part by funds provided for biological and medical research by State of Washington Initiative Measure no. 171.

² Data in this paper are from a thesis submitted by the senior author in partial fulfillment of the requirements for the degree of Doctor of Philosphy.