Subpicogram Determination of Oxytocin by an Enzyme Immunoassay Using Acetylcholinesterase as Label

Pierre‐Guy Marnet, Hervé Volland, P. Pradelles, Jacques Grassi, Marguerite BEAUFILS

Journal of Immunoassay · 1994 · 29 citations · 19 references

Concepts

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.

References

19