Rapid Detection of Porcine DNA by Real-Time Polymerase Chain Reaction (qPCR) on Imported Processed Foods

Agustin Krisna Wardani, Rezaei Reza, Aisyi Sakina Rifani, A. Sutrisno, A. A. Brahmanti
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Abstract

A pair of porcine-specific primers defining a 145 bp region of the mitochondrial D-loop 443 were used to identify the presence of porcine DNA in ten samples of imported instant noodles and soft candies by Real-Time Quantitative Polymerase Chain Reaction (qPCR). This study was performed in three steps: sample preparation, DNA extraction, and DNA amplification using Real-Time PCR. The porcine DNA was amplified at an annealing temperature of 53oC for 39 cycles. The result confirmed that three samples of instant noodles and three soft candies were found to contain porcine D.N.A. This method could effectively authenticate Halal products in processed foods, verify food labelling, and provide consumer protection.
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进口加工食品中猪DNA的实时聚合酶链反应(qPCR)快速检测
采用实时定量聚合酶链式反应(Real-Time Quantitative Polymerase Chain Reaction, qPCR)技术,对10份进口方便面和软糖样品中猪DNA的存在进行了鉴定。本研究分三步进行:样品制备、DNA提取和使用实时荧光定量PCR进行DNA扩增。猪DNA在53℃的退火温度下扩增39个循环。结果证实,3个方便面和3个软糖样品中检出猪dna。该方法可有效鉴别加工食品中的清真产品,验证食品标签,为消费者提供保护。
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