Zhang Shiwei, Lai Xintian, Liu Xiaoqing, Li Yun, Li Bifang, Huang Xiuli, Zhang Qinlei, Chen Wei, Lin Lin, Yang Guowu
Shenzhen Academy of Metrology and Quality Inspection, Shenzhen, P. R. China.
J Immunoassay Immunochem. 2013;34(1):49-60. doi: 10.1080/15321819.2012.680527.
The article presents a sandwich enzyme linked immunosorbent assay (ELISA) for identification of edible bird's nest. The characteristic sialoglycoproteins were found by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and purified by liquid-phase isoelectric focusing (LIEF). According to the analysis, the molecular weight was 106-128 kDa and the isoelectric point was ≤pH 3.0. Two anti-characteristic sialoglycoprotein monoclonal antibodies were produced. The monoclonal antibodies were examined by western-blot assay. One of the monoclonal antibody was used as coating and the other as the enzyme-labeled antibody after being coupled to horseradish peroxidase (HRP). Based on the optimized ELISA condition, the method was established with IC(50) of 1.5 ng/mL, and low cross-reactivity with various fake materials (<0.01%). ELISA provided a suitable means for screening of a large number of samples. The coefficients of variation were between 2.9% and 5.8%.
本文介绍了一种用于鉴定食用燕窝的夹心酶联免疫吸附测定法(ELISA)。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)发现了特征性唾液酸糖蛋白,并通过液相等电聚焦(LIEF)进行了纯化。分析表明,其分子量为106-128 kDa,等电点≤pH 3.0。制备了两种抗特征性唾液酸糖蛋白单克隆抗体。通过蛋白质免疫印迹法检测单克隆抗体。其中一种单克隆抗体用作包被抗体,另一种与辣根过氧化物酶(HRP)偶联后用作酶标抗体。基于优化的ELISA条件,建立的方法IC(50)为1.5 ng/mL,与各种假冒材料的交叉反应率低(<0.01%)。ELISA为大量样品的筛选提供了合适的手段。变异系数在2.9%至5.8%之间。