Abstract
Abstract In these competitive and "sandwich"-type heterogeneous enzyme immunoassays, based on liquid chromatography with electrochemical detection, rabbit immunoglobulin G is used as a model compound. Alkaline phosphatase (EC 3.1.3.1), the labeling enzyme, catalyzes conversion of phenyl phosphate to phenol. After separation on an octyldecylsilane column, the enzyme-generated phenol is detected in a thin-layer cell at a carbon-paste working electrode. The detection limit for phenol is 5.0 nmol/L. The electrode response varies linearly with concentration over a range of three orders of magnitude. For the sandwich-type assay procedure the detection limit is 10 ng/L; the linearity ranges over four orders of magnitude. The detection limit of the competitive immunoassay is 5 micrograms/L. The dynamic range spans two orders of magnitude.
Dates
Type | When |
---|---|
Created | 5 years, 7 months ago (Jan. 16, 2020, 4:11 a.m.) |
Deposited | 5 years, 5 months ago (March 4, 2020, 12:52 a.m.) |
Indexed | 4 months, 2 weeks ago (April 7, 2025, 6:06 p.m.) |
Issued | 39 years, 11 months ago (Sept. 1, 1985) |
Published | 39 years, 11 months ago (Sept. 1, 1985) |
Published Online | 39 years, 11 months ago (Sept. 1, 1985) |
Published Print | 39 years, 11 months ago (Sept. 1, 1985) |
@article{Wehmeyer_1985, title={Heterogeneous enzyme immunoassay with electrochemical detection: competitive and “sandwich”-type immunoassays.}, volume={31}, ISSN={1530-8561}, url={http://dx.doi.org/10.1093/clinchem/31.9.1546}, DOI={10.1093/clinchem/31.9.1546}, number={9}, journal={Clinical Chemistry}, publisher={Oxford University Press (OUP)}, author={Wehmeyer, K R and Halsall, H B and Heineman, W R}, year={1985}, month=sep, pages={1546–1549} }