Aids in the diagnosis of gastrointestinal (GI) infections caused by viral pathogens, including adenovirus (serotypes 40 and 41), astrovirus, norovirus (genogroups 1 and 2), rotavirus, and sapovirus. Use as a sensitive alternative to traditional antigen testing.
Qualitative Polymerase Chain Reaction
Tue, Thu, Sat
New York DOH Approval Status
Transfer 1 mL stool to an unpreserved stool transport vial (ARUP Supply #40910). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. (Min: 0.5 mL).
Ambient: Unacceptable; Refrigerated: 2 weeks; Frozen: 2 weeks
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or test specific nucleic acid in concentrations below the level of detection by this test.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
This assay detects Astrovirus, Sapovirus, Rotavirus, Adenovirus Type 40/41, and differentiates Norovirus Group 1 and Group 2.
|Component Test Code*||Component Chart Name||LOINC|
|0051282||Norovirus 1 by PCR||54905-5|
|0051283||Norovirus 2 by PCR||54906-3|
|2013578||Astrovirus by PCR||92691-5|
|2013580||Sapovirus by PCR|
|2013582||Rotavirus by PCR|
|2013584||Adenovirus 40/41 by PCR||92690-7|