| Literature DB >> 27765258 |
Hassan A Al-Kahtani1, Elsayed A Ismail2, Mohammed Asif Ahmed3.
Abstract
Pork DNA was detected in meat mixtures using both conventional PCR and real-time PCR (RT-PCR). Thirty meat mixtures containing beef, chicken, camel, rabbit, goat and sheep with varying percentage of pork (0%, 1%, 5%, 10%, and 20%) and 75 commercial food products, were analyzed using conventional and RT-PCR to determine the presence of pork DNA. Pork DNA standard curves and cycle threshold (Ct) values were used for quantification. The detection limits for pork DNA in the mixtures were 0.22, 0.047, 0.048, 0.0000037, 0.015ng/μl respectively. Unlike conventional PCR, RT-PCR detected pork DNA in nine processed food samples [chicken sausages (2), chicken luncheon (2), turkey meat loaf, milk chocolate with soft nougat, jelly, cake, and candies] at pork DNA concentrations of 0.0001ng/μl or less.Entities:
Keywords: Agarose (PubChem CID: 11966311); Commercial food products; Ethidium bromide (PubChem CID: 14710); Meat mixtures; Pork adulteration; Real time PCR; TAE buffer (PubChem CID: 21257724)
Mesh:
Year: 2016 PMID: 27765258 DOI: 10.1016/j.foodchem.2016.09.108
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514