Literature DB >> 7710084

Microenzymatic fluorescence assay for serum cholesterol.

M C Gray1, A L Plant, J M Nicholson, W E May.   

Abstract

An enzymatic assay using fluorometric detection for cholesterol determination in serum is described. Results were compared to a conventional enzymatic colorimetric procedure and to the definitive method, which is based on isotope dilution mass spectrometry. Fluorescence detection enhances sensitivity over current colorimetric methods by approximately two orders of magnitude, and the assay response is linear over three orders of magnitude of cholesterol concentration. The reaction is performed in a single step and can be performed with small sample (1 microliter) and reaction (200 microliters) volumes. The fluorescence intensity is stable after a 30-min sample incubation at room temperature. The sensitivity of this fluorescence assay makes it possible to measure subnanomoles of cholesterol, allowing accurate measurement of total cholesterol in 1 microliter of serum or less. This level of sensitivity will also allow measurement of cholesterol in various isolated lipoprotein fractions.

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Year:  1995        PMID: 7710084     DOI: 10.1006/abio.1995.1042

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


  2 in total

1.  Multidimensional profiling of plasma lipoproteins by size exclusion chromatography followed by reverse-phase protein arrays.

Authors:  Gregor Dernick; Stefan Obermüller; Cyrill Mangold; Christine Magg; Hugues Matile; Oliver Gutmann; Elisabeth von der Mark; Corinne Handschin; Cyrille Maugeais; Eric J Niesor
Journal:  J Lipid Res       Date:  2011-10-04       Impact factor: 5.922

2.  Palmitoylcarnitine affects localization of growth associated protein GAP-43 in plasma membrane subdomains and its interaction with Gα(o) in neuroblastoma NB-2a cells.

Authors:  Karolina Tułodziecka; Magdalena Czeredys; Katarzyna A Nałęcz
Journal:  Neurochem Res       Date:  2012-12-09       Impact factor: 3.996

  2 in total

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