DEVELOPMENT, OPTIMIZATION AND USE OF AN ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA) TO MEASURE FACTOR VIII-ANTIGEN UTILIZING MONOCLONAL-ANTIBODIES

被引:3
作者
HORNSEY, VS [1 ]
DRUMMOND, O [1 ]
EAGLESFIELD, P [1 ]
PEPPER, DS [1 ]
PROWSE, CV [1 ]
机构
[1] SCOTTISH NATL BLOOD TRANSFUS SERV,CTR PROT FRACTIONAT,EDINBURGH,SCOTLAND
关键词
VIII AG; ELISA; MONOCLONAL ANTIBODIES;
D O I
10.1111/j.1365-3148.1992.tb00159.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An enzyme linked immunosorbent assay (ELISA) has been developed to measure VIII:Ag in plasma and concentrates. The assay utilizes two commercially available monoclonal antibodies to VIII:Ag and provides an alternative to the established immunoradiometric assay (IRMA). It has the advantage of not requiring the use of radioactive material and human antibodies. The assay sensitivity is 0-006 u/ml and the interassay coefficient of variation is 6.3%. Forty-eight samples with VIII:Ag levels ranging from 0.006 to 1.5 u/ml were assayed by both ELISA and IRMA. The coefficient of correlation between the two assays was 0.89. In addition to measuring human VIII:Ag, it is also possible to detect antigen in several animal plasma and sera.
引用
收藏
页码:223 / 229
页数:7
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