Development and design of a 'ready-to-use' reaction plate for a PCR-based simultaneous detection of animal species used in foods

Autor:	Andreas Butschke, Almuth Spiegelberg, Jutta Zagon, Ines Laube, Lothar W. Kroh, Hermann Broll
Rok vydání:	2007
Předmět:	Detection limit Phosphodiesterase Biology Genome Industrial and Manufacturing Engineering law.invention chemistry.chemical_compound Ingredient chemistry law Food science Cyclic guanosine monophosphate Gene Polymerase chain reaction DNA Food Science
Zdroj:	International Journal of Food Science & Technology. 42:9-17
ISSN:	1365-2621 0950-5423
DOI:	10.1111/j.1365-2621.2006.01154.x
Popis:	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 108 bp in size (exception: duck, 212 bp) 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.
Databáze:	OpenAIRE
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