Literature DB >> 3477964

A fluorometric assay for quantitating phenol sulfotransferase activities in homogenates of cells and tissues.

M Arand1, L W Robertson, F Oesch.   

Abstract

A new, rapid, and sensitive method for assaying phenol sulfotransferase activity toward 2-naphthol is described. The product 2-naphthyl sulfate is quantitated fluorometrically. Optimal wavelengths for excitation and emission were determined by recording the three-dimensional fluorescence spectra of the substrate and the product. The new method is applicable to crude cell or tissue homogenates as well as to further purified preparations. A comparison to another widely used method is given to point out the advantages provided by the new procedure. In particular, sensitivity and accuracy of both methods are evaluated and the influence of interfering substances on both systems is compared. These results clearly indicate the superiority of the new method.

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Year:  1987        PMID: 3477964     DOI: 10.1016/0003-2697(87)90261-2

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  5 in total

1.  Dependency of the in vitro stabilization of differentiated functions in liver parenchymal cells on the type of cell line used for co-culture.

Authors:  D Utesch; F Oesch
Journal:  In Vitro Cell Dev Biol       Date:  1992-03

2.  Phenol sulfotransferase expression in the airways: enzymological and immunohistochemical demonstration.

Authors:  J D Beckmann; J R Spurzem; S I Rennard
Journal:  Cell Tissue Res       Date:  1993-12       Impact factor: 5.249

Review 3.  Recent advances in sulfotransferase enzyme activity assays.

Authors:  Priscilla Paul; Jiraporn Suwan; Jian Liu; Jonathan S Dordick; Robert J Linhardt
Journal:  Anal Bioanal Chem       Date:  2012-04-12       Impact factor: 4.142

4.  Viability, attachment efficiency, and xenobiotic metabolizing enzyme activities are well maintained in EDTA isolated rat liver parenchymal cells after hypothermic preservation for up to 3 days in University of Wisconsin solution.

Authors:  F Oesch; H Abdel-Latif; B Diener
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-09       Impact factor: 2.416

5.  The gap junctional intercellular communication is no prerequisite for the stabilization of xenobiotic metabolizing enzyme activities in primary rat liver parenchymal cells in vitro.

Authors:  M Traiser; B Diener; D Utesch; F Oesch
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-04       Impact factor: 2.416

  5 in total

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