In the past, in order to accurately determine the presence of pinworms in an animal has required a post-mortem direct exam. With the introduction of RADIL's new PCR assay which tests for both Syphacia obvelata and Aspiculuris tetraptera, antemortem testing can now be performed with highly accurate results. RADIL's Pinworm PCR assay is nearly as sensitive as the direct exam and has the advantage that the animal does not need to be euthanized for evaluation. In studies, it was also more sensitive than either of the two antemortem tests (tape test and fecal float).
Pinworm by PCR evaluation will be available beginning December 1, 2009 as part of the Mouse Basic , Mouse Comprehensive and Rat Basic Fecal Panels, as a Helicobacter & Pinworm panel, or as a stand-alone assay. For more information and pricing, please click here.
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At this year's National AALAS Meeting in Denver, Colorado, RADIL
introduced a breakthrough serologic testing technology that will offer clients an increased level of results confidence for the most prevalent mouse and rat agents. MFI2 represents an advanced approach to serologic monitoring for laboratory animal pathogens, providing the highest level of diagnostic accuracy available. By evaluating multiple antigens for each agent, primary and confirmatory testing now occur at the same time, saving time and increasing the predictive value of the final results. Clients will begin seeing multiple antigens reported on case reports as of December 1, 2009.
For more information regarding MFI2, please visit the Serology section of this site.
( for more info click here )Feces: Fecal pellets for PCR evaluation should be collected with clean gloves or sterile forceps and placed in individually labeled sterile containers. Two to three pellets per animal are adequate. If multiple animals of the same microbiologic status are to be evaluated, up to 10 fecal pellets can be pooled and tested as one sample. If fecal pellets from multiple animals are to be collected, gloves should be changed or forceps should be replaced between animals to prevent cross-contamination. Alternatively, forceps can be wiped clean and immersed in a dilute bleach (10%) solution for 10 minutes prior to reuse. Fecal pellets for identification of Helicobacters and mnv should be shipped by an overnight carrier, but do not need to be chilled or frozen. Fecal pellets for identification of other viruses should be frozen and shipped to our laboratory by overnight courier with sufficient dry ice so that samples remain frozen during shipment.