Rapid immunofiltration assay of Newcastle disease virus using a silicon sensor

A rapid nonradioactive sandwich immunoassay which utilizes biotin-streptavidin mediated filtration capture of immune complexes in conjunction with a silicon sensor was developed for the detection of virus. Using purified Newcastle disease virus as a model, the lower limits of detection (LOD) were de...

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Veröffentlicht in:Journal of immunological methods 1993-11, Vol.166 (1), p.123-131
Hauptverfasser: Lee, William E., Thompson, H.Gail, Hall, John G., Fulton, R.Elaine, Wong, Jonathan P.
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Sprache:eng
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Zusammenfassung:A rapid nonradioactive sandwich immunoassay which utilizes biotin-streptavidin mediated filtration capture of immune complexes in conjunction with a silicon sensor was developed for the detection of virus. Using purified Newcastle disease virus as a model, the lower limits of detection (LOD) were determined for a number of immunoassay configurations employing both monoclonal and polyclonal antibodies. The LODs ranged from 1.3 ng/ml (sample volume of 100 μl) for an incubation of 60 min to 400 ng/ml for a 1 min incubation. The sandwich immune complexes were formed from one-step incubation of antibody and antigen. No ‘hook’ effects were observed over a wide range of analyte concentrations. The assays were easy to perform and required a total time equal to the incubation period plus about 5 min. The assay format is suitable for virus, bacteria and protein antigens. New assays can be developed and optimized readily, often within 1 day.
ISSN:0022-1759
1872-7905
DOI:10.1016/0022-1759(93)90336-6