Bacterial Genome Detection - PCR/NAT Multiplex Detection Method for Gastrointestinal Pathogens (548)

Samples:

4 samples of 0.3 ml

Sample properties:

Lyophilised cell suspension

Additional Information:

In order to take into account the usually very different pathogen coverage of commercially available multiplex PCR/NAT concepts, each of the parameters listed above is certified separately as part of the evaluation. Only results from multiplex PCR/NAT test systems with a precisely specified test/kit designation are accepted. The parallel use of singleplex PCR/NAT detection methods for individual pathogens in the panel is not certified. The relatively broad spectrum of pathogen-specific EQA programmes for bacterial genome detection PCR/NAT is still available for this purpose.

Requirement for EQAS/PT according to Rili-BÄK

Certificate Validity: 12 months

Not subject to Rili-BÄK

Parameters:

Mixtures of 0 to 4 of the different pathogens specified in the panel are to be expected in the respective individual samples:

 

Selection of

Aeromonas spp., Campylobacter spp., Clostridium difficile (toxinogen), Enterohemorrhagic E. coli (EHEC / STEC), Enterotoxigenic E. coli (ETEC), Enteropathogenic E. coli (EPEC), Enteroaggregative E. coli (EAEC), Escherichia coli O157, Plesiomonas spp., Salmonella spp., Shigella/EIEC, Vibrio spp., Yersinia enterocolitica

Certificate Validity: 12 months

Shipping Information:

Shipping not cooled

Safety Information:

Process as patient sample material

EQAS/PT Experts: