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Elisa to quantify hexanal-protein adducts in a meat model system.

机译:Elisa量化肉类模型系统中的己醛蛋白质加合物。

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Monoclonal antibodies (MAb) were produced to hexanal-bovine serum albumin conjugates. An indirect competitive ELISA was developed with a detection range of 1-50 ng of hexanal/mL. Hexanal conjugated to three different proteins was recognized, whereas free hexanal and the native proteins were not detected. The antibody cross-reacted with pentanal, heptanal, and 2-trans-hexenal conjugated to chicken serum albumin (CSA) with cross-reactivities of 37.9, 76.6, and 45.0%, respectively. There was no cross-reactivity with propanal, butanal, octanal, and nonanal conjugated to CSA. The hexanal content of a meat model system was determined using MAb and polyclonal antibody-based ELISAs and compared with analysis by a dynamic headspace gas chromatographic (HS-GC) method and a thiobarbituric acid reactive substances (TBARS) assay. Both ELISAs showed strong correlations with the HS-GC and TBARS methods. ELISAs may be a fast and simple alternative to GC for monitoring lipid oxidation in meat.
机译:产生了针对牛-牛血清白蛋白结合物的单克隆抗体(MAb)。开发了一种间接竞争ELISA,检测范围为1-50 ng己醛/ mL。识别与三种不同蛋白质缀合的己醛,而未检测到游离己醛和天然蛋白质。该抗体与结合至鸡血清白蛋白(CSA)的戊醛,庚醛和2-反己酮发生交叉反应,交叉反应率分别为37.9%,76.6和45.0%。与与CSA共轭的丙醛,丁醛,octanal和nonanal没有交叉反应。使用MAb和基于多克隆抗体的ELISA确定了肉类模型系统的己醛含量,并与动态顶空气相色谱(HS-GC)方法和硫代巴比妥酸反应性物质(TBARS)分析相比较。两种ELISA均显示与HS-GC和TBARS方法密切相关。 ELISA可能是GC监测肉类脂质氧化的一种快速简便的替代方法。

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