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首页> 外文期刊>Experimental and therapeutic medicine >Establishment and primary clinical application of competitive inhibition for measurement of augmenter of liver regeneration.
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Establishment and primary clinical application of competitive inhibition for measurement of augmenter of liver regeneration.

机译:用于测量肝脏再生增强剂的竞争性抑制作用的建立和初步临床应用。

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摘要

The aim of the present study was to establish a quantitative method for the measurement of serum human augmenter of liver regeneration (hALR) using competitive inhibition that is applicable in the clinic. A monoclonal antibody to hALR was used as the primary antibody and the pure hALR protein was used as a standard for competition with Eu(3+)-labeled hALR (Eu(3+)-hALR) to plot a standard curve. Serum samples from 90 patients with various liver diseases due to hepatitis B virus (HBV) infection were used for a competitive reaction with Eu(3+)-hALR. A regression analysis of the results was performed using the standard curve to calculate the serum concentration of hALR. The minimum detectable value using direct competitive measurement established by Eu(3+)-hALR was 1 ng/ml, with a positive linear correlation within the range of 200 ng/ml. In the sera of the 90 patients, the hALR level in the severe hepatitis group was the highest, followed by that in the acute hepatitis group. The serum hALR levels in the cirrhosis and chronic hepatitis groups were significantly higher compared with those in the normal control groups (P<0.01). The direct competitive measurement method of serum hALR established in the present study has high sensitivity, specificity, stability and reliability, meets clinical requirements and may be used as potential index in clinical tests.
机译:本研究的目的是建立一种定量方法,该方法使用竞争性抑制作用来测量血清人肝再生增强剂(hALR),该方法可用于临床。将抗hALR的单克隆抗体用作第一抗体,并将纯hALR蛋白用作与Eu(3+)标记的hALR(Eu(3 +)-hALR)竞争的标准,以绘制标准曲线。来自90名患有乙型肝炎病毒(HBV)感染的各种肝病患者的血清样本用于与Eu(3 +)-hALR的竞争性反应。使用标准曲线对结果进行回归分析,以计算hALR的血清浓度。使用由Eu(3 +)-hALR建立的直接竞争测量法得出的最小可检测值为1 ng / ml,线性正相关在200 ng / ml的范围内。在90例患者的血清中,重型肝炎组的hALR水平最高,其次是急性肝炎组。肝硬化和慢性肝炎组的血清hALR水平明显高于正常对照组(P <0.01)。本研究建立的血清hALR直接竞争测量方法具有较高的灵敏度,特异性,稳定性和可靠性,符合临床要求,可作为临床检测的潜在指标。

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