Literature DB >> 2231181

Optimal conditions for protease use in the assay of serum mitochondrial aspartate aminotransferase.

H Okabe1, Y Uji, H Sugiuchi, Y Watazu, Y Shirahase, N Kaneda.   

Abstract

The optimal conditions for selective proteolytic inactivation of cytosolic aspartate aminotransferase (c-AST) to determine mitochondrial aspartate aminotransferase (m-AST) in serum were studied. Protease 401 was found to be effective over a pH range of 6.0-10.0. A pH of 9.5 with 0.5% albumin in the reagent mixture was determined to be optimal for inactivation of c-AST and preservation of m-AST, lactic dehydrogenase (LDH), and malic dehydrogenase (MDH) in the assay procedure. The presence of serum endogenous protein inhibitors such as alpha 1-antitrypsin and alpha 2-macroglobin did not inhibit protease 401.

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Year:  1990        PMID: 2231181     DOI: 10.1002/jcla.1860040507

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  1 in total

1.  Simple reversed-phase HPLC method with spectrophotometric detection for measuring acetaminophen-protein adducts in rat liver samples.

Authors:  Miteshkumar Acharya; Cesar A Lau-Cam
Journal:  ScientificWorldJournal       Date:  2012-04-19
  1 in total

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