A noncompetitive enzyme immunoassay method (hetero-two-site enzyme immunoassay) for salmon calcitonin (SCT) and its usability for the pharmacokinetic study are described. The method in brief proceeds as follows: centrifugal filtration through a polysaccharide membrane to remove plasma proteins, biot
Noncompetitive enzyme immunoassay for the measurement of bronchial inhibitor in biological fluids
โ Scribed by J.M. Tournier; J. Jacquot; P. Sadoul; J.G. Bieth
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 419 KB
- Volume
- 131
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
An enzyme-linked immunosorbent assay (ELISA) of bronchial inhibitor using rabbit antibronchial inhibitor antibody-coated polystyrene balls as the solid-phase antibody and peroxidaselabeled antibody as the conjugate is described. A crude antibody fraction is used for coating the solid phase. The assay can be run within 8 h and gives reproducible results in the range of 6 to 60 rig/l of bronchial inhibitor (mean within-run coefficient of variation, 7%). It can detect bronchial inhibitor concentrations as low as 2 &I (lo-" M) and recovery of varying amounts of bronchial inhibitor added to bronchial liquids is greater than 90%. This enzyme immunoassay appears to be a convenient way to quantify bronchial inhibitor in biological fluids such as serum, sputum, or bronchoalveolar lavage fluid.
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