Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1984 Jan;19(1):34-8.
doi: 10.1128/jcm.19.1.34-38.1984.

Comparative evaluation of different enzyme-linked immunosorbent assay systems for the detection of staphylococcal enterotoxins A, B, C, and D

Comparative Study

Comparative evaluation of different enzyme-linked immunosorbent assay systems for the detection of staphylococcal enterotoxins A, B, C, and D

H Fey et al. J Clin Microbiol. 1984 Jan.

Abstract

We compared four versions of the enzyme-linked immunosorbent assay for their suitability for detecting staphylococcal enterotoxins. The sandwich with labeled antibody proved to be the best. We used it with a sorbent consisting of antibody-coated polystyrene spheres reacted with 20 ml of food extract. The sensitivity of the test was 0.1 ng of enterotoxin per ml, which is far below clinical relevance. The succinimidyl-pyridyl-dithio-propionate enzyme coupling method of Pharmacia was superior to the two-step glutaraldehyde technique. Interfering protein A was eliminated by the simple addition of normal rabbit serum to the extracts. A diagnostic kit is now available.

PubMed Disclaimer

References

    1. Appl Microbiol. 1971 Nov;22(5):837-41 - PubMed
    1. Zentralbl Bakteriol Mikrobiol Hyg A. 1983 Feb;253(4):466-75 - PubMed
    1. J Agric Food Chem. 1974 Jan-Feb;22(1):9-13 - PubMed
    1. Can J Microbiol. 1978 Apr;24(4):436-9 - PubMed
    1. Appl Microbiol. 1974 Jan;27(1):83-5 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources