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HelpTest Code DENVP Dengue Virus Antibody/Antigen Panel, Serum
Additional Codes
| Mayo Test ID | COPIA Test Code | EPIC Test Codes | |
|---|---|---|---|
| DENVP | DENVP-Dengue Virus Antibody/Antigen Panel, Serum | LAB1150 | DENGUE VIRUS AB/AG PROFILE |
Useful For
Aiding in the diagnosis of dengue virus infection by detection of IgM and IgG antibodies and the nonstructural protein 1 (NS1)
Profile Information
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| DENG | Dengue Virus Ab, IgG, S | No | Yes |
| DENM | Dengue Virus Ab, IgM, S | No | Yes |
| DENS1 | Dengue NS1 Ag, S | Yes, (DNSAG) | Yes |
| INT69 | Dengue Interpretation | No | Yes |
Reporting Name
Dengue Virus Ab/Ag Panel, SSpecimen Type
SerumSpecimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into plastic vial.
Specimen Minimum Volume
0.8 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Serum | Refrigerated (preferred) | 14 days | |
| Frozen | 14 days |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
| Heat-inactivated specimen | Reject |
Reference Values
IgG: Negative
IgM: Negative
NS1: Negative
Reference values apply to all ages.
Day(s) Performed
Tuesday
Report Available
Same day/1 to 7 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
86790 x 3
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| DENVP | Dengue Virus Ab/Ag Panel, S | 104595-4 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| INT69 | Dengue Interpretation | 69048-7 |
| DENG | Dengue Virus Ab, IgG, S | 29661-6 |
| DENM | Dengue Virus Ab, IgM, S | 29663-2 |
| DENS1 | Dengue NS1 Ag, S | 75377-2 |
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.