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首页> 外文期刊>American Journal of Veterinary Research >Development and validation of a sandwich ELISA for use in measuring concentrations of canine surfactant protein A in serum of dogs
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Development and validation of a sandwich ELISA for use in measuring concentrations of canine surfactant protein A in serum of dogs

机译:夹心酶联免疫吸附测定法的开发和验证,该测定法用于测量犬血清中犬表面活性剂蛋白A的浓度

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摘要

Objective-To develop and evaluate a sandwich ELISA incorporating rabbit antiserum specific for canine surfactant protein A (SP-A) for use in measuring concentrations of SP-A in serum of dogs.Sample-Serum samples obtained from 6 healthy dogs and 3 dogs with pulmonary disease.Procedures-Rabbit antiserum was prepared against purified canine SP-A. The IgG fraction was isolated via protein G affinity chromatography and was then biotinylated. The sandwich ELISA was performed by use of anti-SP-A antibody (IgG) preabsorbed with sera from healthy dogs. Validity of the ELISA was confirmed by determination of the detection limit, precision, reproducibility, and accuracy. Serum SP-A concentrations were measured in 6 healthy dogs and 3 dogs with pulmonary disease.Results-Detection limit of the ELISA was 2.0 ng/mL. Within- and between-assay coefficients of variation ranged from 3.8% to 14.1% and from 15.5% to 35.6%, respectively. The observed-to-expected recovery ratio ranged from 77.1% to 89.9%. Serum SP-A concentrations measured by use of the ELISA were <= 2.3 ng/mL in the 6 healthy dogs, 25.6 ng/mL in a dog with severe cardiac pulmonary edema, 8.3 ng/mL in a dog with pneumonia, and 10.1 ng/mL in a dog with lung lobe torsion.Conclusions and Clinical Relevance-The sandwich ELISA was found to be useful for measuring purified canine SP-A concentrations and canine SP-A concentrations in serum samples. The ELISA was precise, reproducible, and accurate. The ELISA may be beneficial in assessing serum concentrations of canine SP-A as a potential biomarker of pulmonary diseases in dogs. (Am J Vet Res 2011;72:833-837)
机译:目的-开发和评估一种夹心ELISA试剂盒,该抗体结合了针对犬表面活性剂蛋白A(SP-A)的兔抗血清,用于测量狗血清中SP-A的浓度。从6只健康狗和3只狗获得的血清样品针对纯化的犬SP-A制备了兔抗血清程序。通过蛋白G亲和层析分离IgG级分,然后进行生物素化。夹心ELISA通过使用预先从健康犬血清中吸收的抗SP-A抗体(IgG)进行。通过确定检测限,精密度,可重复性和准确性来确认ELISA的有效性。测定了6只健康犬和3只肺部疾病犬的血清SP-A浓度。ELISA检测结果为2.0 ng / mL。批内和批间变异系数分别为3.8%至14.1%和15.5%至35.6%。观察到预期的回收率范围为77.1%至89.9%。通过ELISA测量的血清SP-A浓度在6只健康犬中为≤2.3ng / mL,在具有严重心脏肺水肿的犬中为25.6 ng / mL,在肺炎犬中为8.3 ng / mL,并为10.1 ng / mL在患有肺叶扭转的狗中。结论和临床意义-发现夹心ELISA可用于测量血清样品中纯化的犬SP-A浓度和犬SP-A浓度。 ELISA精确,可重复且准确。 ELISA可能有助于评估犬SP-A的血清浓度,将其作为犬肺部疾病的潜在生物标记。 (Am J Vet Res 2011; 72:833-837)

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