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Use of genetically modified organisms (GMOs) in international food production has resulted in religious and health issues, especially among Muslim consumers. There is a need to have good analyses that will guarantee the authenticity and safety of the halal food products. Objectives: To identify and determine the concentration of GM contamination in both raw and processed foodstuff samples using a sensitive quantitative polymerase chain reaction (qPCR) method. Methods: Certified Reference Material (CRM-BF410ep Soya Bean) was used to construct a qPCR standard curve by 10-fold serial dilution (0.1% 0.01% 0.001% 0.0001%). GMO-positive cabbage seeds were added to processed food (China noodles, mixed spices, rice protein) and unprocessed food (brown rice, basmati rice, IRRI-6 rice). The NOS terminator sequence has been measured using qPCR to amplify DNA by extracting it with a commercial kit, quantifying it, and subsequently analyzing the DNA sample. Efficiency and limits of detection. Results: NOS terminator sequence was easily identified in a concentration of 0.001% and the mean Ct values were similar to the CRM standard. The statistical analysis (p.05) showed that there is no significant differentiation between the CRM and spiked samples, which proves the accuracy and reproducibility of the method at low concentrations of DNA. Conclusions: The tested qPCR technique proved to be very sensitive in the detection of GM contamination in various food matrices at 0.001 percent. Conclusions: This method will aid in halal food authentication, and a reliable molecular tool will help in avoiding accidental intake of GM haram ingredients.
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Nadeem et al. (2025) studied this question.
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