Time filter

Source Type

Sun W.,Chinese Academy of Agricultural Sciences | Sun W.,Jilin Provincial Key Laboratory for Molecular Biology | Li G.,Chinese Academy of Agricultural Sciences | Li G.,Jilin Provincial Key Laboratory for Molecular Biology | And 14 more authors.
Asian Journal of Animal and Veterinary Advances | Year: 2012

The study was to develop a Polymerase Chain Reaction (PCR) assay for specific detection of mink meat using designed pairs of primers based on mitochondria1 D-loop. Mmk meat is used as fraud ingredients of false mutton or dog meat in meat markets. This study was conducted to establish Polymerase Chain Reaction (PCR) method for the sensitive and specific detection of mink (Mustela uison) DNA in meat products. Six pairs of primers were designed from tandem repeat region of D-loop in mitochondria after alignment of the available sequences in the GenBank database. The specific pair of primers chosen from the six designed pairs by PCR generated specific fragments of 343 bp in length for mink. The specificity of detection was conducted with DNA samples of mink, blue fox, dog, raccoon dog, swine, sheep. Then amplification of positive reaction was observed only in mink species. In this study, no adverse effects of cooking and autoclaving were found on amplification of mink DNA fragments. Then the detection limit was found to be less than 1% in mixed meat products. The PCR method described in this study proved to be very sensitive and reliable in mink DNA identification. Thus, it could be considered as a further improvement method for the detection of mink DNA in meat products processed under different manufacturing conhtions. © 2012 Academic Journals Inc.

Loading Jilin Provincial Key Laboratory for Molecular Biology collaborators
Loading Jilin Provincial Key Laboratory for Molecular Biology collaborators