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血浆或血清中的C4别型分析:在常规实验室中的应用

C4 allotyping on plasma or serum: application to routine laboratories.

作者信息

Zhang W J, Kay P H, Cobain T J, Dawkins R L

机构信息

Department of Clinical Immunology, Royal Perth Hospital, Queen Elizabeth II Medical Centre, Western Australia.

出版信息

Hum Immunol. 1988 Mar;21(3):165-71. doi: 10.1016/0198-8859(88)90068-7.

Abstract

Allotypes of the fourth component of complement (C4) can be detected by electrophoresis and immunofixation after treatment of EDTA plasma with neuraminidase (NAse). We have assessed the value of additional treatment with carboxypeptidase B (CPseB). Following treatment with CPseB + NAse, each allele is resolved into a single band, permitting clear definition of overlapping bands seen following treatment with NAse alone. More importantly, C4 allotypes can be determined using stored heparinized plasma or serum. Most C4 null alleles can be assigned without requiring family studies. The approach described is suitable for routine use by tissue typing laboratories.

摘要

用神经氨酸酶(NAse)处理EDTA血浆后,通过电泳和免疫固定法可检测补体第四成分(C4)的同种异型。我们评估了用羧肽酶B(CPseB)进行额外处理的价值。用CPseB + NAse处理后,每个等位基因都可解析为一条单一的条带,从而能够清晰地界定仅用NAse处理后出现的重叠条带。更重要的是,可使用储存的肝素化血浆或血清来确定C4同种异型。大多数C4无效等位基因无需进行家系研究即可确定。所描述的方法适用于组织分型实验室的常规使用。

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