Mahi Mahi IgE
Use
This test measures the specific IgE antibodies to mahi mahi in human serum. The presence of specific IgE to mahi mahi indicates a sensitization to this specific allergen, which is associated with an increased risk of allergic reactions. The test is useful in the clinical diagnosis of fish allergy, aiding in the management of patients who may be at risk for allergic reactions upon exposure to mahi mahi.
Special Instructions
Ordering requires a specific serum sample collection. Ensure that the specimen is collected in a plain red-top tube or serum gel tube, then spun down and the serum is refrigerated in a plastic vial before sending for testing. Note that the test is available for order for New York State clients.
Limitations
This test was developed and its performance characteristics determined by Eurofins Viracor. It has not been cleared or approved by the U.S. FDA. As a result, it should be used for clinical purposes following the defined guidelines. Assay performance can be affected by gross lipemia, which is a cause for specimen rejection.
New York Approved
Methodology
Immunoassay (FEIA)
Biomarkers
LOINC Codes
- 82570-3
- 82570-3
- 103121-0
Result Turnaround Time
3-6 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.5 mL
Container
Red or SST
Collection Instructions
Draw blood in a plain red-top tube(s), serum gel tube is acceptable. Spin down and send 0.5 mL of serum refrigerated in a plastic vial.
Causes for Rejection
Gross lipemia
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 28 days |
| Refrigerated | 28 days |
| Frozen | 365 days |