首页> 外文期刊>Journal of Agricultural and Food Chemistry >Quantitative Tetraplex Real-Time Polymerase Chain Reaction Assay with TaqMan Probes Discriminates Cattle, Buffalo, and Porcine Materials in Food Chain
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Quantitative Tetraplex Real-Time Polymerase Chain Reaction Assay with TaqMan Probes Discriminates Cattle, Buffalo, and Porcine Materials in Food Chain

机译:用Taqman探针定量四络实时聚合酶链反应测定判别食物链中的牛,水牛和猪材料

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摘要

Cattle, buffalo, and porcine materials are widely adulterated, and their quantification might safeguard health, religious, economic, and social sanctity. Recently, conventional polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (RFLP) assays have been documented but they are just suitable for identification, cannot quantify adulterations. We described here a quantitative tetraplex real-time PCR assay with TaqMan Probes to quantify contributions from cattle, buffalo, and porcine materials simultaneously. Amplicon-sizes were very short (106-, 90-, and 146-bp for cattle, buffalo, and porcine) because longer targets could be broken down, bringing serious ambiguity in molecular diagnostics. False negative detection was eliminated through an endogenous control (141-bp site of eukaryotic 18S rRNA). Analysis of 27 frankfurters and 27 meatballs reflected 84-115% target recovery at 0.1-10% adulterations. Finally, a test of 36 commercial products revealed 71% beef frankfurters, 100% meatballs, and 85% burgers contained buffalo adulteration, but no porcine was found in beef products.
机译:牛,水牛和猪材料广泛掺杂,它们的量化可能会保障健康,宗教,经济和社会神圣性。最近,已经记载了常规的聚合酶链反应(PCR)和PCR限制性片段长度多态性(RFLP)测定,但它们仅适用于鉴定,不能量化掺杂。这里我们在此描述了具有Taqman探针的定量四络实时PCR测定,以量化牛,水牛和猪材料的贡献。扩增子尺寸非常短(106-,90-和146-BP用于牛,水牛和猪),因为较长的目标可能会被分解,在分子诊断中带来严重的模糊性。通过内源性对照(141bp的真核18s rRNA)消除了假阴性检测。分析27个法兰克福和27个肉丸,反映了0.1-10%掺假的84-115%的目标回收。最后,对36个商业产品的考验揭示了71%的牛肉法兰克福,100%肉丸,85%汉堡含有水牛掺杂,但在牛肉产品中没有发现猪。

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