首页> 外文期刊>Animal Feed Science and Technology >Application of species-specific polymerase chain reaction assays to verify the labeling of quail (Coturnix coturnix), pheasant (Phasianus colchicus) and ostrich (Struthio camelus) in pet foods.
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Application of species-specific polymerase chain reaction assays to verify the labeling of quail (Coturnix coturnix), pheasant (Phasianus colchicus) and ostrich (Struthio camelus) in pet foods.

机译:物种特异性聚合酶链反应法在验证鹌鹑( Coturnix coturnix ),野鸡( Phasianus colchicus )和鸵鸟( Struthio camelus )的标签中的应用>)在宠物食品中。

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摘要

Species-specific polymerase chain reaction (PCR) assays have been applied to verify the labeling of pet foods containing quail, pheasant, and ostrich. The method combines the use of quail, pheasant, ostrich, chicken, duck, pig and fish specific primers that amplify small fragments (amplicons <200 base pairs) of the mitochondrial 12S rRNA gene and a positive control primer pair that amplifies a 141bp fragment of the nuclear 18S rRNA gene from eukaryotic DNA. The applicability of the assay was tested through the analysis of 100 commercial dog and cat food products. The reported PCR technique successfully detected the presence of the target species in 88 of the analyzed samples. However, the target species was not detected in 12 samples indicating a possible fraud in the labeling of these products. The results obtained suggest that the reported PCR method may represent a suitable tool for the detection of pet food mislabeling
机译:物种特异性聚合酶链反应(PCR)分析已应用于验证包含鹌鹑,野鸡和鸵鸟的宠物食品的标签。该方法结合了鹌鹑,野鸡,鸵鸟,鸡,鸭,猪和鱼的特异性引物的使用,该引物可扩增线粒体12S rRNA基因的小片段(扩增子<200个碱基对)和一个阳性对照引物对,可扩增线粒体12S rRNA基因的141bp片段。真核DNA中的核18S rRNA基因。通过分析100种市售猫狗食品,测试了该方法的适用性。报道的PCR技术成功地检测了88个分析样品中目标物种的存在。但是,在12个样品中未检测到目标物种,表明这些产品的标签可能存在欺诈行为。获得的结果表明,所报道的PCR方法可能是检测宠物食品标签错误的合适工具。

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