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一种用于全血中猪C反应蛋白定量的时间分辨免疫荧光分析方法。

A time-resolved immunofluorometric assay for porcine C-reactive protein quantification in whole blood.

作者信息

Martinez-Subiela S, Eckersall P D, Campbell F M, Parra M D, Fuentes P, Ceron J J

机构信息

Department of Animal Medicine and Surgery, University of Murcia, 30100 Espinardo, Murcia, Spain.

出版信息

Luminescence. 2007 May-Jun;22(3):171-6. doi: 10.1002/bio.945.

Abstract

A time-resolved immunofluorometric assay (TR-IFMA) for C-reactive protein (CRP) determination in whole blood of pigs was developed and validated. CRP was isolated from porcine acute-phase serum by affinity chromatography on agarose, coupled with phosphorylethanolamine and polyclonal antibodies to porcine CRP were purified from antiserum raised in sheep immunized with porcine CRP. Intra- and inter-assay coefficients of variation (CVs) were in the range 3.13-7.19% and 7.06-15.66%, respectively, showing good precision. The assay measured the CRP values in a proportional and linear manner (r=0.99); additionally, CRP concentrations measured in whole blood by the present TR-IFMA and in serum by an established immunoturbidimetric assay were highly correlated (R(2)=0.97). The limit of detection of the method was 0.0028 mg/L. Significantly lower CRP concentrations were observed after 7 days of sample storage at 4 degrees C. The injection of turpentine oil caused a significant increase in CRP concentrations and significantly higher CRP concentrations were observed in pigs with pathological processes compared to healthy animals.

摘要

开发并验证了一种用于测定猪全血中C反应蛋白(CRP)的时间分辨免疫荧光测定法(TR-IFMA)。通过琼脂糖亲和色谱从猪急性期血清中分离CRP,将其与磷酸乙醇胺偶联,并从用猪CRP免疫的绵羊产生的抗血清中纯化抗猪CRP的多克隆抗体。批内和批间变异系数(CV)分别在3.13-7.19%和7.06-15.66%范围内,显示出良好的精密度。该测定法以成比例和线性方式测量CRP值(r=0.99);此外,用本TR-IFMA在全血中测量的CRP浓度与用既定免疫比浊法在血清中测量的CRP浓度高度相关(R(2)=0.97)。该方法的检测限为0.0028 mg/L。在4℃下储存7天后观察到CRP浓度显著降低。注射松节油导致CRP浓度显著升高,与健康动物相比,在患有病理过程的猪中观察到显著更高的CRP浓度。

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