• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

两种商用酶联免疫吸附测定(ELISA)试剂盒和三种自行研发的实时聚合酶链反应(PCR)检测方法用于检测食品中潜在致敏性芥末的验证与比较。

Validation and comparison of two commercial ELISA kits and three in-house developed real-time PCR assays for the detection of potentially allergenic mustard in food.

作者信息

Palle-Reisch Monika, Hochegger Rupert, Štumr Stepan, Korycanova Kveta, Cichna-Markl Margit

机构信息

Department of Analytical Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria; AGES, Austrian Agency for Health and Food Safety, Institute for Food Safety, Department of Molecular Biology and Microbiology, Spargelfeldstraße 191, 1220 Vienna, Austria.

AGES, Austrian Agency for Health and Food Safety, Institute for Food Safety, Department of Molecular Biology and Microbiology, Spargelfeldstraße 191, 1220 Vienna, Austria.

出版信息

Food Chem. 2015 May 1;174:75-81. doi: 10.1016/j.foodchem.2014.10.132. Epub 2014 Nov 3.

DOI:10.1016/j.foodchem.2014.10.132
PMID:25529654
Abstract

The study compares the applicability of two commercial mustard ELISA kits (Mustard ELISA Kit-specific and Mustard ELISA Kit-total) and three in-house developed real-time PCR assays (singleplex assay for white mustard, singleplex assay for black/brown mustard and duplex assay for the detection of white, black and brown mustard). Analyses of raw and brewed model sausages containing white and black/brown mustard in the range from 1 to 50 ppm indicate that both ELISAs and the three real-time PCR assays allow the detection of traces of mustard in raw and in brewed sausages. The ELISAs were found to be more sensitive than the real-time PCR assays. When the ELISAs and real-time PCR assays were applied to the analysis of 15 commercial foodstuffs differing in their labelling concerning mustard, in one sample mustard was detected with both ELISAs and the three real-time PCR assays although mustard was not indicated on the food ingredient list.

摘要

该研究比较了两种商用芥末酶联免疫吸附测定试剂盒(特异性芥末酶联免疫吸附测定试剂盒和总芥末酶联免疫吸附测定试剂盒)以及三种内部开发的实时聚合酶链反应检测方法(用于白芥末的单重检测方法、用于黑/棕芥末的单重检测方法以及用于检测白芥末、黑芥末和棕芥末的双重检测方法)的适用性。对含有浓度范围为1至50 ppm的白芥末和黑/棕芥末的生香肠和煮制香肠模型进行分析表明,酶联免疫吸附测定和三种实时聚合酶链反应检测方法均能检测出生香肠和煮制香肠中的微量芥末。结果发现,酶联免疫吸附测定比实时聚合酶链反应检测方法更灵敏。当将酶联免疫吸附测定和实时聚合酶链反应检测方法应用于分析15种在芥末标签方面存在差异的商用食品时,在一个样品中,两种酶联免疫吸附测定方法和三种实时聚合酶链反应检测方法均检测到了芥末,尽管食品成分表中未标明含有芥末。

相似文献

1
Validation and comparison of two commercial ELISA kits and three in-house developed real-time PCR assays for the detection of potentially allergenic mustard in food.两种商用酶联免疫吸附测定(ELISA)试剂盒和三种自行研发的实时聚合酶链反应(PCR)检测方法用于检测食品中潜在致敏性芥末的验证与比较。
Food Chem. 2015 May 1;174:75-81. doi: 10.1016/j.foodchem.2014.10.132. Epub 2014 Nov 3.
2
Development and validation of a duplex real-time PCR assay for the simultaneous detection of three mustard species (Sinapis alba, Brassica nigra and Brassica juncea) in food.建立并验证一种用于同时检测食品中三种芥菜类蔬菜(白芥、黑芥和芥菜)的双重实时荧光 PCR 方法。
Food Chem. 2014 Jun 15;153:66-73. doi: 10.1016/j.foodchem.2013.12.035. Epub 2013 Dec 12.
3
Development and validation of a duplex real-time PCR method for the simultaneous detection of celery and white mustard in food.开发并验证了一种用于同时检测食品中芹菜和白芥菜的双重实时 PCR 方法。
Food Chem. 2013 Nov 1;141(1):229-35. doi: 10.1016/j.foodchem.2013.02.088. Epub 2013 Mar 7.
4
Development and validation of a triplex real-time PCR assay for the simultaneous detection of three mustard species and three celery varieties in food.建立并验证三重实时荧光 PCR 方法,用于同时检测食品中三种芥菜物种和三种芹菜品种。
Food Chem. 2015 Oct 1;184:46-56. doi: 10.1016/j.foodchem.2015.03.049. Epub 2015 Mar 20.
5
Development and validation of a real-time PCR method for the simultaneous detection of black mustard (Brassica nigra) and brown mustard (Brassica juncea) in food.开发并验证一种实时 PCR 方法,用于同时检测食品中的黑芥菜(Brassica nigra)和褐芥菜(Brassica juncea)。
Food Chem. 2013 May 1;138(1):348-55. doi: 10.1016/j.foodchem.2012.10.055. Epub 2012 Nov 8.
6
Development and validation of a real-time PCR method for the detection of white mustard (Sinapis alba) in foods.用于检测食品中白芥(白芥属)的实时荧光定量PCR方法的建立与验证
J Agric Food Chem. 2010 Nov 10;58(21):11193-200. doi: 10.1021/jf102452a. Epub 2010 Oct 6.
7
Validation and comparison of a sandwich ELISA, two competitive ELISAs and a real-time PCR method for the detection of lupine in food.验证和比较夹心 ELISA、两种竞争 ELISA 和实时 PCR 方法在食品中检测羽扇豆的效果。
Food Chem. 2013 Nov 1;141(1):407-18. doi: 10.1016/j.foodchem.2013.02.091. Epub 2013 Mar 14.
8
Sandwich enzyme-linked immunosorbent assay (ELISA) for detection of mustard in foods.用于检测食品中芥子气的夹心酶联免疫吸附测定(ELISA)。
J Food Sci. 2008 May;73(4):T62-8. doi: 10.1111/j.1750-3841.2008.00725.x.
9
Quantitative detection of hazelnut (Corylus avellana) in cookies: ELISA versus real-time PCR.曲奇中榛子(榛属)的定量检测:ELISA 与实时 PCR 法。
J Agric Food Chem. 2011 Nov 9;59(21):11395-402. doi: 10.1021/jf202167b. Epub 2011 Oct 14.
10
Quantitative detection of allergenic protein Sin a 1 from yellow mustard (Sinapis alba L.) seeds using enzyme-linked immunosorbent assay.采用酶联免疫吸附测定法对黄芥籽(白芥)中的致敏蛋白Sin a 1进行定量检测。
J Agric Food Chem. 2008 Feb 27;56(4):1184-92. doi: 10.1021/jf072660u. Epub 2008 Jan 25.

引用本文的文献

1
1D-, 2D-Gel Electrophoresis, Immunoblotting, and Enzyme-Linked Immunosorbent Assay (ELISA) for the Study of Food Allergens.1D-、2D-凝胶电泳、免疫印迹和酶联免疫吸附测定(ELISA)在食物过敏原研究中的应用。
Methods Mol Biol. 2024;2717:123-142. doi: 10.1007/978-1-0716-3453-0_8.
2
Simultaneous detection of fruit allergen-coding genes in tomato, apple, peach and kiwi through multiplex PCR.通过多重PCR同时检测番茄、苹果、桃子和猕猴桃中的水果过敏原编码基因。
Food Sci Biotechnol. 2019 Mar 16;28(5):1593-1598. doi: 10.1007/s10068-019-00591-y. eCollection 2019 Oct.
3
Rapid on-site detection of shrimp allergen tropomyosin using a novel ultrafast PCR system.
使用新型超快PCR系统快速现场检测虾过敏原原肌球蛋白
Food Sci Biotechnol. 2018 Sep 27;28(2):591-597. doi: 10.1007/s10068-018-0479-x. eCollection 2019 Apr.