Peroxidase-Labelled Monoclonal Antibodies for use in Enzyme Immunoassay
- 1 December 1987
- journal article
- research article
- Published by Taylor & Francis in Journal of Immunoassay
- Vol. 8 (4) , 297-307
- https://doi.org/10.1080/15321818708057029
Abstract
Desirable characteristics of enzyme-antibody conjugates for use in enzyme immunoassay are labelling uniformity, permanent availability and stability. The use of monoclonal antibodies (MCABS) for preparation of enzyme conjugates, in place of poly-clonal antibodies, ensures labelling uniformity and permanent availability. The problem of stability still exists. Monoclonal antibody-horseradish peroxidase (McAB-HREQ) conjugates produced in our laboratory showed variable stability. After extensive testing of McAB-HRPO conjugates it became obvious that sodium borohydride, used as a reducing agent, did not result in the production of stable conjugates without enzyme pretreatment with fluorodinitrobenzene (FDNB). Ascorbic acid or ethanolamine used as the reducing agent, resulted in McAB-HRPO conjugates which were stable for periods of ten months or more when stored filter sterilized at 4°C.This publication has 6 references indexed in Scilit:
- A comparison of the ability of β-galactosidase and horseradish peroxidase enzyme-antibody conjugates to detect specific antibodiesJournal of Immunological Methods, 1979
- Peroxidase Labelling of Antibodies for Use in Enzyme ImmunoassayBiochemical Society Transactions, 1979
- Development of an enzyme immunoassay for human placental lactogen using labelled antibodiesJournal of Immunological Methods, 1976
- PEROXIDASE-LABELED ANTIBODY A NEW METHOD OF CONJUGATIONJournal of Histochemistry & Cytochemistry, 1974
- Hypoferremia in Mice and Its Application to the Bioassay of EndotoxinJournal of Bacteriology, 1965