Use to detect and differentiate dengue subtypes 1-4.
Qualitative Polymerase Chain Reaction
New York DOH Approval Status
Lavender (EDTA), Pink (K2EDTA), or Serum Separator Tube (SST).
Separate serum or plasma from cells. Transfer 1 mL serum or plasma to a sterile container. (Min: 0.5mL)
Specimen source required.
Ambient: 24 hours; Refrigerated: 5 days; Frozen: 2 weeks
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or of 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 and differentiates Dengue subtypes 1-4.
|Component Test Code*||Component Chart Name||LOINC|
|2013295||Dengue by PCR, Source||31208-2|
|2013296||Dengue Type 1 by PCR||60262-3|
|2013297||Dengue Type 2 by PCR||60420-7|
|2013298||Dengue Type 3 by PCR||60419-9|
|2013299||Dengue Type 4 by PCR||60418-1|
- Breakbone Fever