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RADIL Introduces Pinworm by PCR Testing
11.19.2009

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. 

( for more info click here )
MFI2 - The next generation in serology testing
11.19.2009

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 )



Elizabeth C. Bryda
Associate Professor
RADIL - University of Missouri
Email Address: brydae@missouri.edu
Phone #: 573-882-5504
Fax #: 573-884-7521

Research emphasis: Our laboratory takes a comparative medicine approach to studying human disorders by using a variety of animal models of disease. The current emphasis in the lab is on the study of polycystic kidney disease and hereditary deafness. Using both rodent and zebra fish models, we are interested in characterizing disease-causing genes and their protein products in order to elucidate the molecular pathways in which these genes/proteins participate. This knowledge will allow a better understanding of both normal and abnormal development in the kidney or the inner ear and may ultimately lead to the development of targeted therapeutics. Another focus of the laboratory is to develop tools and diagnostics in the field of laboratory animal medicine. We have developed panels of multiplexed microsatellite markers for improved genetic characterization and monitoring of laboratory animals, including mouse, rat, and pig. We are currently developing efficient and cost-effective methods to validate and authenticate cell lines from any species, including human cell lines.
University of Missouri-Columbia
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