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Development and design of a 'ready-to-use'reaction plate for a PCR-based simultaneous detection of animal species used in foods
Different TaqManTM-polymerase chain reaction systems have been developed, which allow the detection of even minute amounts of beef, pork, lamb, goat, chicken, turkey and duck in processed foods. The species-specific systems are able to amplify DNA regions with no more than 108bp in size (exception:...
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Published in: | International journal of food science & technology 2007-01, Vol.42 (1), p.9-17 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | Different TaqManTM-polymerase chain reaction systems have been developed, which allow the detection of even minute amounts of beef, pork, lamb, goat, chicken, turkey and duck in processed foods. The species-specific systems are able to amplify DNA regions with no more than 108bp in size (exception: duck, 212bp) located on the single-copy genes cyclic guanosine monophosphate (cyclic GMP) phosphodiesterase, ryanodine receptor and interleukin-2 precursor. The parallel detection of the common ingredient 'meat' produced from mammals and poultry was based on the amplification of a region of the myostatin gene. The limit of detection was determined to be ten genome copies for each system. The relative SD under repeatability condition was below 30%. In addition, a 'ready-to-use'reaction plate has been developed, which makes it possible to investigate the presence of the seven animal species in parallel after a single real-time run. |
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ISSN: | 0950-5423 |
DOI: | 10.1111/j.1365-2621.2006.01154.x |