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通过酶联免疫吸附测定(ELISA)检测血小板抗体。与间接免疫荧光测定的比较研究。

Detection of platelet antibodies by enzyme-linked immunosorbent assay (ELISA). Comparative studies with the indirect immunofluorescence assay.

作者信息

Horai S, Claas F H, van Rood J J

出版信息

Immunol Lett. 1981 Aug;3(3):155-8. doi: 10.1016/0165-2478(81)90119-x.

Abstract

A newly developed enzyme-linked immunosorbent assay (ELISA) for the detection of platelet antibodies was compared with the platelet immunofluorescence test (PIF). A good correlation was found between both assays. However, ELISA seems to be more sensitive than PIF. Some sera reacted only in ELISA whereas no sera were found that were negative in ELISA and positive in PIF. When comparing the antibody titres, ELISA is at least 8 times more sensitive than PIF.

摘要

一种新开发的用于检测血小板抗体的酶联免疫吸附测定(ELISA)与血小板免疫荧光试验(PIF)进行了比较。两种测定方法之间发现有良好的相关性。然而,ELISA似乎比PIF更敏感。一些血清仅在ELISA中出现反应,而未发现ELISA呈阴性而PIF呈阳性的血清。在比较抗体滴度时,ELISA的敏感性至少是PIF的8倍。

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