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首页> 外文期刊>Journal of AOAC International >Evaluation of Qualitative and Quantitative Immunoassays To Detect Barley Contamination in Gluten-Free Beer with Confirmation Using LC/MS/MS
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Evaluation of Qualitative and Quantitative Immunoassays To Detect Barley Contamination in Gluten-Free Beer with Confirmation Using LC/MS/MS

机译:使用LC / MS / MS进行鉴定的定性和定量免疫分析检测无麸质啤酒中大麦污染的评估

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摘要

To meet the need for the detection and quantitation of barley gluten in beer, qualitative screening and quantitative immunoassays based on the monoclonal antigluten antibody 401/21 (Skerritt) were validated in a single laboratory. Sample replicates were tested at each stage of beer production using multiple yeast strains and methods of end-stage protein removal. Quantitation was performed using barley-specific standards based on barley flour extracts. Immunoassay results were confirmed using LC/MS/MS for barley-specific peptides. The LOD for the qualitative screening test was 5 mg/L barley gluten. Recovery for the barley-spiked worts ranged from 81 to 128% in the quantitative ELISA assay; the LOD was 1 mg/L, and the LOQ was 5 mg/L. Both screening and confirmation methods were found to be fit for the purposes of detection of low levels of barley gluten in beer.
机译:为了满足检测和定量啤酒中大麦麸质的需要,在单个实验室中验证了基于单克隆抗麸质抗体401/21(Skerritt)的定性筛选和定量免疫测定。在啤酒生产的每个阶段,使用多种酵母菌株和最终蛋白质去除方法对样品重复进行测试。使用基于大麦粉提取物的大麦特定标准品进行定量。使用大麦特异性肽的LC / MS / MS确认了免疫分析结果。定性筛选测试的LOD为5 mg / L大麦麸质。在定量ELISA分析中,大麦加味麦芽汁的回收率在81%到128%之间。 LOD <1 mg / L,LOQ为5 mg / L。发现筛选和确认方法都适合于检测啤酒中低水平的大麦面筋。

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