Ortea, I., Pascoal, A., Canas, B., Gallardo, J.M., Barros-Velazquez, J. and Calo-Mata, P. (2012) Food Authentication of Commercially-Relevant Shrimo and Prawn Species: From Classical Methods to Foodomics. Electrophoresis, 33, 2201-2211.
https://doi.org/10.1002/elps.201100576

has been cited by the following article:

• TITLE: Specificity of Various Mitochondrial DNA (mtDNA), ND5, D-Loop, and Cty-b DNA Primers in Detecting Pig (Sus scrofa) DNA Fragments

  AUTHORS: Joni Kusnadi, Noval Audi Ashari, Estri Laras Arumingtyas

  KEYWORDS: Cyt-b, D-Loop, mt-DNA, ND5, Pigs, Pork, Specificity

  JOURNAL NAME: American Journal of Molecular Biology, Vol.10 No.3, June 1, 2020

  ABSTRACT: Polymerase Chain Reaction (PCR) is an accurate, simple and fast analytical method. This technique is widely used in the identification of meat adulteration and meat-based processed food products. Three Mitochondrial DNA (mt-DNA) primers NADH Dehydrogenase sub unit 5 (ND5), D-Loop, and Cytochrome b (Cyt-b) were tested for their specificity in detecting of pig (Sus scrofa) DNA fragments. DNA genome from 6 meat samples (pork, beef, goat, lamb, and chicken) was amplified by PCR technique using three pairs of primers (ND5, D-Loop, and Cyt-b) and sequenced. The results of amplification using the three primers produced specific DNA bands with the lengths of 232 bp, 951 bp, and 404 bp, respectively. Comparison results with ND5, D-Loop, and Cyt-b gene sequences resulted in similarity values of 100%, 97%, and 99%, respectively. These showed that the mt-DNA primers of ND5, D-Loop, and Cyt-b genes can be recommended as specific primers in detecting pig (Sus scrofa) DNA fragments.