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Subpicogram determination of oxytocin by an enzyme immunoassay using acetylcholinesterase as label

Authors :
M. Beaufils
Marnet Pg
Philippe Pradelles
Jacques Grassi
H. Volland
Laboratoire de recherches sur la traite
Institut National de la Recherche Agronomique (INRA)
ProdInra, Migration
Source :
Journal of Immunoassay and Immunochemistry, Journal of Immunoassay and Immunochemistry, Taylor & Francis, 1994, 15 (1), pp.35-53
Publication Year :
1994

Abstract

The pure tetrameric form of Acetylcholinesterase (EC-3.1.1.7) from the electric eel electrophorus electricus has been covalently coupled to oxytocin. This conjugate has been used as tracer in a heterologous competitive immunoassay. Microtiter plates coated with a mouse monoclonal anti-rabbit immunoglobulin antibody were used to separate bound and free moieties of the tracer. Acetylcholinesterase activity bound to the solid phase was measured by a colorimetric assay. The minimum detectable concentration was 0.075 pg/well (ie 1.5 pg/ml) and precision was less than 8% at concentration above 0.15 pg/well. An extraction step improved sensitivity up to 10 times with good recoveries. To assess the validity of this assay, basal levels of oxytocin were measured during the oestrous cycle of a cow.

Details

ISSN :
01971522, 15321819, and 15324230
Volume :
15
Issue :
1
Database :
OpenAIRE
Journal :
Journal of immunoassay
Accession number :
edsair.doi.dedup.....c239717e3c4bd3fd986c0130237d70e8