1996
DOI: 10.2508/chikusan.67.900
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Species Identification of Meats and Meat Products by PCR

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Cited by 14 publications
(11 citation statements)
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“…However, these methods have such an inferior reproducibility or low efficiency of simultaneous detection for all kinds of meat species. Multiplex PCR (Dalmasso et al, 2003;Fei et al, 1996;Matsunaga et al, 1999) was a new method that could simultaneously amplify template mixture and decrease the detection cost, conquering the weakness of single PCR detecting only one template once. However, multiplex PCR method had several disadvantages such as complex system with many primers, low amplified efficiency and no identical efficiency on different templates, which restricted the commercial application in detecting meat species.…”
Section: Introductionmentioning
confidence: 99%
“…However, these methods have such an inferior reproducibility or low efficiency of simultaneous detection for all kinds of meat species. Multiplex PCR (Dalmasso et al, 2003;Fei et al, 1996;Matsunaga et al, 1999) was a new method that could simultaneously amplify template mixture and decrease the detection cost, conquering the weakness of single PCR detecting only one template once. However, multiplex PCR method had several disadvantages such as complex system with many primers, low amplified efficiency and no identical efficiency on different templates, which restricted the commercial application in detecting meat species.…”
Section: Introductionmentioning
confidence: 99%
“…Biomolecular techniques have been extensively used because of high degree of specificity and being applicable to heat processed products (Momcilovic & Rasooly, 2000). Among them, DNA hybridization (Chikuni, Ozutsumi, Koishikawa, & Kato, 1990;Wintero, Thomsen, & Davies, 1990) and PCR methods (Chikuni, Tabata, Kosugiyama, Momma, & Saito, 1994;Fei et al, 1996) have been used for identification of meats and meat products. DNA hybridization generally are more complicated and inadequate than PCR, which easily amplifies target regions of template DNA in a much shorter time (Saiki et al, 1985), and thus is suitable for meat identification.…”
Section: Introductionmentioning
confidence: 99%
“…This assay tested with many other animal and plant species used in the formation of meatball and is found to be simple, stable, sensitive and specific to detect dog meat in processed food which is very important for halal authentication purposes. Fei et al (1996); Monteil-Sosa et al (2000) and Mane et al (2009) tried to differentiate the chicken from other meat species by designing a primer pair on the basis of mitochondrial D-loop gene to amplify 442bp of DNA fragments followed by subjecting the resulted fragments to digestion by HaeIII and Sau3AI enzymes where amplification of 442 bp DNA fragment was observed only in chicken even after cross testing with red meat species investigated (cattle, buffalo, sheep, goat, pig, duck, guinea fowl, turkey and quail) indicating the high specificity of this PCR assay for chicken meat that provide a useful tool for detecting of meat species even in ad-mixed meat and meat products under different processing conditions.…”
Section: Restriction Fragment Length Polymorphism (Pcr-rflp)mentioning
confidence: 99%