Two commonly used methodologies for species detection within processed meat products are real-time polymerase chain reaction (PCR), a DNA-based method, and enzyme-linked immunosorbent assay (ELISA), a protein-based method. In this study, a real-time PCR assay was compared to a commercial ELISA kit based on sensitivity, specificity, agreement among duplicate samples, cost, time, and ease of use. Fifteen reference samples containing known percentages (0.1–99.9%, w/w) of pork and beef were analyzed in duplicate using both methods. Thirty commercial products, including sausages, pet treats, and canned meats, were also tested in duplicate with each method. Reference sample analysis showed real-time PCR was able to detect pork in duplicate sample...
Identification of meat species in processed meat products is a major problem in meat technology to p...
The development of highly sensitive and quantitative tools to identify undeclared pork meat is very ...
In the thesis development of suitable routine methods ELISA and PCR for the identification of muscle...
Two commonly used methodologies for species detection within processed meat products are real-time p...
An important factor in the detection of falsification is the control of the composition of the meat ...
Objective Detection of adulteration in processed meats is an important issue for some countries due ...
The identification of meat species in food products and pharmaceuticals is vital to minimize food ad...
The need for reliable and sensitive methods for meat species identification in ground and comminuted...
The problem of adulterated ingredients in processed food products is widely observed in the food ind...
In this study, we describe an inter-laboratory collaborative ring trial validation of species-specif...
Although most consumers are sensitive about the origin of the meat they consume, adulteration of mea...
Bovine and porcine are poultry meat that consumed worldwide particularly in Southeast Asia.Both of t...
In this study, pork-specific real-time PCR assay is developed for Halal authentication. Three specif...
Multiplex polymerase chain reaction (M-PCR) assay was applied to processed and raw meats for the ide...
Species identification in meat products has grown in interest in recent years since these foodstuffs...
Identification of meat species in processed meat products is a major problem in meat technology to p...
The development of highly sensitive and quantitative tools to identify undeclared pork meat is very ...
In the thesis development of suitable routine methods ELISA and PCR for the identification of muscle...
Two commonly used methodologies for species detection within processed meat products are real-time p...
An important factor in the detection of falsification is the control of the composition of the meat ...
Objective Detection of adulteration in processed meats is an important issue for some countries due ...
The identification of meat species in food products and pharmaceuticals is vital to minimize food ad...
The need for reliable and sensitive methods for meat species identification in ground and comminuted...
The problem of adulterated ingredients in processed food products is widely observed in the food ind...
In this study, we describe an inter-laboratory collaborative ring trial validation of species-specif...
Although most consumers are sensitive about the origin of the meat they consume, adulteration of mea...
Bovine and porcine are poultry meat that consumed worldwide particularly in Southeast Asia.Both of t...
In this study, pork-specific real-time PCR assay is developed for Halal authentication. Three specif...
Multiplex polymerase chain reaction (M-PCR) assay was applied to processed and raw meats for the ide...
Species identification in meat products has grown in interest in recent years since these foodstuffs...
Identification of meat species in processed meat products is a major problem in meat technology to p...
The development of highly sensitive and quantitative tools to identify undeclared pork meat is very ...
In the thesis development of suitable routine methods ELISA and PCR for the identification of muscle...