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通过抗体夹心酶联免疫吸附测定法鉴定埃及伊蚊的血餐。

Identification of blood meals in Aedes aegypti by antibody sandwich enzyme-linked immunosorbent assay.

作者信息

Chow E, Wirtz R A, Scott T W

机构信息

Department of Entomology, University of Maryland, College Park 20742.

出版信息

J Am Mosq Control Assoc. 1993 Jun;9(2):196-205.

PMID:8350077
Abstract

A comparative study of 3 ELISA protocols was performed for host blood meal identification in Aedes aegypti. In the sandwich-B ELISA, which used a combination of heavy and heavy+light chain conjugates, specificity was improved to such a degree that conjugates no longer required cross-adsorption with heterologous sera. Using the sandwich-B assay, human blood meals in laboratory reared Ae. aegypti could be detected longer after feeding (100% at 32 h and 80% at 42 h) than with a direct assay (100% at 20 h). Efficacy of the sandwich-B and direct ELISAs in field analyses was studied in parallel) using 80 field collected mosquitoes from Thailand. The sandwich-B assay was superior (88% detection rate) to the direct assay (41% detection rate) and was thus selected as the method of choice for future field studies.

摘要

为了鉴定埃及伊蚊的宿主血餐,对3种酶联免疫吸附测定(ELISA)方案进行了比较研究。在使用重链和重链+轻链缀合物组合的夹心-B ELISA中,特异性提高到了这样的程度,即缀合物不再需要与异源血清进行交叉吸附。使用夹心-B检测法,实验室饲养的埃及伊蚊在进食后更长时间仍可检测到人类血餐(32小时时为100%,42小时时为80%),而直接检测法(20小时时为100%)则不然。同时使用从泰国采集的80只野外蚊子研究了夹心-B ELISA和直接ELISA在野外分析中的效果。夹心-B检测法(检测率88%)优于直接检测法(检测率41%),因此被选为未来野外研究的首选方法。

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