Dengue Virus IgG
The DENV DetectTM IgG ELISA test for exposure to Dengue Virus (DENV) is an ELISA assay system for the detection of IgG antibodies in human serum to Dengue-derived recombinant antigen (DENRA). This test is to aid in the diagnosis of human exposure to the Dengue virus.
ProcedureBiological matrix is diluted in buffer and incubated in microtiter wells coated with monoclonal antibody bound to recombinant Dengue antigen (DENRA) and normal cellular antigen (NCA) separately. Wells are then treated with a human IgG-specific monoclonal antibody labeled with horseradish peroxidase. After a second incubation, the wells are incubated with tetramethylbenzidine. An acidic stopping solution is then added and the degree of enzymatic turnover of the substrate is measured by absorbance at 450 nanometers. The ratio of each sample's paired DENRA and NCA absorbances are used to calculate the Immune Status Ratio (ISR). Compared to threshold points, the ISR value determines whether antibodies to Dengue virus are present.
SpecificitySerological cross-reactivity across the flavivirus group is common. Certain sera from patients infected with Japanese Encephalitis, West Nile, and/or Saint Louis Viruses may give false positive results.
2-3 business days from receipt of specimen
| Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
|---|---|---|---|---|---|---|
| serum | 5219239 | 86790 | Yes | 1 mL |
Less than 1.65 ISR: Negative - No significant level of detectable dengue fever virus IgG antibody. 1.65-2.84 ISR: Equivocal - Questionable presence of antibodies. Repeat testing in 10-14 days may be helpful. Greater than 2.84 ISR: Positive - IgG antibody to dengue fever virus detected, which may indicate a current or past infection. |
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Less than 1.65 ISR: Negative - No significant level of detectable dengue fever virus IgG antibody.
1.65-2.84 ISR: Equivocal - Questionable presence of antibodies. Repeat testing in 10-14 days may be helpful.
Greater than 2.84 ISR: Positive - IgG antibody to dengue fever virus detected, which may indicate a current or past infection.
Shipping
Ship Monday through Friday. Label Friday shipments for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor Eurofins test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Viracor Eurofins, 18000 W 99th St. Ste, #10, Lenexa, KS 66219.
Causes for RejectionSpecimen types other than serum. Grossly lipemic or hemolyzed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
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