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荧光免疫分析的发展。

The development of fluorescence immunoassays.

作者信息

Barnard G

机构信息

Department of Obstetrics and Gynaecology, King's College School of Medicine and Dentistry, Denmark Hill, London.

出版信息

Prog Clin Biol Res. 1988;285:15-37.

PMID:3068674
Abstract

Radioactive markers have been of inestimable value in the establishment of immunoassays for compounds of analytical interest. It is anticipated, however, that the trend towards the development of alternative fluorescence immunoassays will continue. For example, where extreme assay sensitivity is not required, the development of simple nonseparation FIAs (e.g., fluorescence polarization FIA) will continue. However, the lanthanide chelates can be measured with high sensitivity and the specific activity of the labelled conjugates may exceed that of conjugates prepared with radioisotopes. Consequently, this approach has great potential for achieving higher sensitivity than can be obtained by conventional IRMA procedures. The components of an assay are harmless and easily disposed of. The labelled materials are very stable, showing no significant deterioration after storage for more than a year. The approach has been successfully exploited in the development of two-site immunofluorometric assays of proteins and direct, competitive binding assays of haptens. In the future, it is anticipated that the introduction of new fluorescent probes and appropriate instrumentation will facilitate the introduction of tests which may be performed in the ward, in the outpatient clinic, or in the home.

摘要

放射性标记物在建立针对具有分析意义的化合物的免疫测定方法中具有不可估量的价值。然而,可以预期的是,开发替代荧光免疫测定方法的趋势将持续下去。例如,在不需要极高测定灵敏度的情况下,简单的非分离荧光免疫测定法(如荧光偏振免疫测定法)的开发仍将继续。然而,镧系螯合物能够以高灵敏度进行测定,并且标记结合物的比活性可能超过用放射性同位素制备的结合物。因此,这种方法具有极大的潜力,能够实现比传统免疫放射分析程序更高的灵敏度。该测定方法的成分无害且易于处理。标记材料非常稳定,储存一年多后无明显降解。这种方法已成功应用于蛋白质的双位点免疫荧光测定法以及半抗原的直接竞争结合测定法的开发。未来,可以预期,新型荧光探针和合适仪器的引入将有助于开展可在病房、门诊或家中进行的检测。

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