Fluorescence polarization immunoassay:: Detection of antibody to Brucella abortus

被引:41
|
作者
Nielsen, K
Lin, M
Gall, D
Jolley, M
机构
[1] Canadian Food Inspect Agcy, Anim Dis Res Inst, Nepean, ON K2H 8P9, Canada
[2] Jolley Consulting & Res Inc, Grayslake, IL 60030 USA
来源
关键词
D O I
10.1006/meth.2000.1038
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fluorescence polarization immunoassay (FPA) is a homogeneous immunoassay useful for rapid and accurate detection of antibody or antigen. The principle of the assay is that a fluorescent dye (attached to an antigen or an antibody fragment) can be excited by plane-polarized light at the appropriate wavelength. As a rule, a small molecule rotates faster when in solution than a larger molecule, The rotation rate may be assessed by measuring light intensity in the vertical and horizontal planes. Generally, the time it takes a molecule to rotate through a given angle is an indication of its size. When a small molecule that rotates rapidly is bound to a larger molecule, the rotation rate is decreased and this decrease is measured. Because it Is a primary antigen-antibody interaction, the rate of reaction is very rapid and usually a result may be obtained in minutes. This technology was applied to the detection of antibody to Brucella abortus in serum and milk, providing for the first time a rapid primary binding assay that is cost effective for use in the field. (C) 2000 Academic Press.
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页码:71 / 76
页数:6
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