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Research Article| Volume 73, ISSUE 1, P166-172, January 1969

An isotopic assay for alanine transaminase

  • Allen L. Pollock
    Affiliations
    From the Laboratory of Pharmacology, The Children's Cancer Research Foundation, Harvard Medical School Boston, Mass., USA

    From the Department of Biology, Northeastern University Boston, Mass., USA
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  • Ellen Loehr
    Affiliations
    From the Laboratory of Pharmacology, The Children's Cancer Research Foundation, Harvard Medical School Boston, Mass., USA

    From the Department of Biology, Northeastern University Boston, Mass., USA
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  • Dewayne Roberts
    Correspondence
    Reprint requests: Dr. DeWayne Roberts, St. Jude Children's Research Hospital, 332 North Lauderdale, Memphis, Tenn. 38101.
    Affiliations
    From the Laboratory of Pharmacology, The Children's Cancer Research Foundation, Harvard Medical School Boston, Mass., USA

    From the Department of Biology, Northeastern University Boston, Mass., USA
    Search for articles by this author
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      Abstract

      A simple, isotopic method for the assay of alanine transaminase has been developed involving toluene extraction of the 2,4-dinitrophenylhydrazone of pyruvate-14C formed from alanine-14C. The method has been applied to rat liver, rat serum, human serum, and partially purified enzyme from human liver. A high degree of correlation was observed between the isotopic assay and the method of Reitman and Frankel for the measurement of alanine transaminase activity in human serum.
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