A sensitive chemiluminescent sandwich-type enzyme immunoassay for hen egg lysozyme was developed. The assay was performed on polystyrene microtitre plates using immobilized specific polyclonal rabbit antibody against lysozyme, a peroxidase conjugate and the H202/luminol-enhanced chemiluminescence de
Enhanced chemiluminescent immunoassay for aldosterone
β Scribed by Hubl, W. ;Thorpe, G. H. G. ;Hofmann, F. ;Meissner, D. ;Thiele, H. J.
- Publisher
- John Wiley and Sons
- Year
- 1990
- Weight
- 230 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0884-3996
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A solid phase immunoassay for aldosterone using enhanced chemiluminescent detection has been developed. Monoclonal antibodies against aldosterone were used for the immune reaction and compared with polyclonal antibodies. Uniform Protein A coated polystyrene tubes were used as solid phase for the monoclonal antibody and second (antiβrabbit) antibody coated tubes for the polyclonal antibody. Horseradish peroxidase was covalently linked to aldosterone as enzyme label. Optimum conditions were established for the generation and measurement of the luminescent reactions using luminol, pβiodophenol as enhancer and hydrogen peroxide.
The advantages of this assay are the high sensitivity with a detection limit of 100fg/tube, the prolonged luminescence signal with a simplification of the measurement (simpler detectors, external start pipetting) and the short measure time with the possibility of repeated measurement. The coefficients of variation were 4.2%β7.3% in the concentration range 140β1180 pmol/l. The assay showed a significant correlation (r = 0.91) with the ELISA.
The aldosterone concentrations in plasma and saliva of patients with Conn's syndrome were significantly increased, and in patients with Addison's disease were found near the detection limit.
π SIMILAR VOLUMES
An enhanced chemiluminescent immunoassay is described for the measurement of allergen-specific IgE antibodies. The assay is demonstrated for pollen from four grass species. A comparison was made between results obtained by this method and those obtained by the radioallergosorbent (RAST) procedure; a
A simple chemiluminescent immunoassay (CLIA) for urinary albumin has been developed based on the use of a chemiluminescent acridinium ester-labelled human albumin and a commercially available antiserum. It includes t w o incubation steps and a second polyethylene glycol-assisted antibody separation.
Acetylcholine and choline chemiluminescent assays have limitations when these compounds are detected in small areas of mammalian nervous tissue. Use of 7-dimethylaminonaphthalene-1.2-dicarbonic acid hydrazide (7-DMAN), instead of luminol, gives a threefold increase in emitted light in the chemilumin
A highly sensitive and specific chemiluminescent immunoassay (CLIA) was developed for quantification of growth hormone (GH) in salmonid species. The CLIA for salmon GH was performed using the sandwich method with anti-GH IgG as the first antibody and chemiluminescent acridinium ester-labelled specif
Enhanced chemiluminescent quantitation of horseradish peroxidase labels has been incorporated into assays performed on the ES 600 automatic immunoassay analyser. The rapid end-point produced excellent dos+response curves and potential savings in total assay times of up to 40%.