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抗原检测酶联免疫吸附测定:血清预处理以减少特定宿主抗体的干扰。

Antigen detection ELISAs: pretreatment of serum to reduce interference by specific host antibodies.

作者信息

More S J, Copeman D B

机构信息

Graduate School of Tropical Veterinary Science and Agriculture, James Cook University of North Queensland, Townsville, Australia.

出版信息

Trop Med Parasitol. 1991 Jun;42(2):91-4.

PMID:1716780
Abstract

The pretreatment of serum to reduce interference by specific host antibodies was investigated as a means of improving the sensitivity of antigen detection ELISAs whilst screening serum samples. Four antigen detection assays based on monoclonal antibodies directed against antigens of the bovine filariid Onchocerca gibsoni were used in this study and, of these, three assays suffered a dramatic drop in sensitivity when detecting male O. gibsoni antigen in the presence of bovine serum as compared with antigen in buffer. A number of methods for pretreating serum to eliminate the problem of antibody interference with antigen detection were attempted, including heat and alkali treatments, detergent treatment of heat treated samples and the use of a reducing agent. The pretreatment of serum by boiling for 5 minutes in the presence of an equal volume of 0.1 M Na2EDTA pH 4.0 and recovery of the supernatant fluid following centrifugation at 16000 g was the most effective method of restoring the sensitivity of each of these three assays whilst screening bovine serum. Pretreatment of serum using this method produced up to a 512-fold increase in sensitivity compared with results obtained in assays with non-treated serum.

摘要

在筛选血清样本时,研究了血清预处理以减少特定宿主抗体干扰的方法,作为提高抗原检测酶联免疫吸附测定(ELISA)灵敏度的一种手段。本研究使用了四种基于针对牛丝状线虫吉氏盘尾丝虫抗原的单克隆抗体的抗原检测试验,其中三种试验在检测牛血清存在下的雄性吉氏盘尾丝虫抗原时,与缓冲液中的抗原相比,灵敏度急剧下降。尝试了多种血清预处理方法以消除抗体干扰抗原检测的问题,包括热处理、碱处理、对热处理样本进行去污剂处理以及使用还原剂。在等体积的0.1M pH 4.0的Na2EDTA存在下将血清煮沸5分钟,然后在16000g离心后回收上清液,这种血清预处理方法是在筛选牛血清时恢复这三种试验中每种试验灵敏度的最有效方法。与未处理血清的试验结果相比,使用该方法预处理血清可使灵敏度提高多达512倍。

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