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利用单克隆抗体对人补体成分C9进行免疫放射分析。

Immunoradiometric assay for human complement component C9 utilising monoclonal antibodies.

作者信息

Morgan B P, Campbell A K, Luzio J P, Siddle K

出版信息

Clin Chim Acta. 1983 Oct 31;134(1-2):85-94. doi: 10.1016/0009-8981(83)90187-0.

Abstract

A two-site immunoradiometric assay for human C9 has been developed. The assay utilised two non-competing monoclonal antibodies to C9 in a single incubation assay protocol. The detection limit of the assay was 0.1 ng (1.4 X 10(-15) moles) in a sample volume of 100 microliters. Using this assay the C9 concentration in normal human plasma was 60.2 +/- 14.9 mg/l (mean +/- 1 standard deviation, 8.5 X 10(-10) mol/l. Significantly elevated levels were found in the plasma of patients with rheumatoid arthritis (90.4 +/- 19.9 mg/l, mean +/- 1 SD). Measurements of C9 in cerebrospinal fluid and synovial fluid were also performed. The low levels of C9 in cerebrospinal fluid (less than 1 mg/l), undetectable by previously available assay methods, were easily measurable with this highly sensitive assay.

摘要

已开发出一种用于检测人C9的双位点免疫放射分析方法。该分析方法在单一孵育分析方案中使用了两种针对C9的非竞争性单克隆抗体。在100微升样本体积中,该分析方法的检测限为0.1纳克(1.4×10⁻¹⁵摩尔)。使用该分析方法,正常人血浆中C9浓度为60.2±14.9毫克/升(平均值±1标准差,8.5×10⁻¹⁰摩尔/升)。类风湿性关节炎患者血浆中C9水平显著升高(90.4±19.9毫克/升,平均值±1标准差)。还对脑脊液和滑液中的C9进行了测量。脑脊液中C9的低水平(低于1毫克/升),以前的检测方法无法检测到,而使用这种高灵敏度分析方法很容易测量。

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