实时聚合酶链反应检测加工牛肉产品中猪DNA

T. Septiani
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引用次数: 3

摘要

肉类是富含蛋白质的食物原料之一,非素食者消费最多。食用清真食品是每个穆斯林的义务。通常被猪肉污染的肉类加工产品。PCR技术是一种常用的产品真伪认证技术,其中最常用的是RT-PCR技术。选择RT-PCR技术作为鉴定方法,因为RT-PCR技术对鲜肉和加工产品中的猪DNA检测具有较高的准确度。RT-PCR是在聚合酶的帮助下,在两个寡核苷酸限制的特定区域进行扩增的技术。退火是RT-PCR分析的第一个过程,主要附着在DNA模板上,决定了DNA的特异性和产生的数量。本研究采用提取试剂盒和检测试剂盒对肉丸中的猪DNA进行分析。本研究获得的结果来自完整的DNA样本,DNA纯度在1.82到1.93之间。所有样本中有三个含有猪的DNA。扩增曲线显示阳性样品,这是探针与猪基因反应时特异性形成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of Porcine DNA in Processed Beef Products Using Real Time – Polymerase Chain Reaction
Meat is one of food materials which has protein source and mostlyconsumed by non-vegetarian. Consuming halal food is an obligation for every Muslim. Meat processed products usually contaminated by pork. One of technique that is often chosen as an authentication process for proofing halalness of the product is PCR technique, one of PCR technique which most commonly used is RT-PCR. RT-PCR technique was chosen as identification method because it has high accuration for detection of porcine DNA in fresh meat and processed products. RT-PCR is the amplification technique in the specific regions that are restricted by two oligonucleotide with the help of polymerase enzymes. Annealing is the first process of RT-PCR analysis who was primary attachment to the DNA template that determines the specificity and amount of DNA produced. In this study, extraction kit and detection kit were used for analysis Porcine DNA in meatballs. The results obtained from this study were from whole DNA samples, which had DNA purity ranging from 1.82 to 1.93. From the all samples three of them containing porcine DNA. The positive samples shown from amplification curves who was specifically formed when probes reacts with porcine gene.
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