Coconut, IgE, Serum
Use
This test is useful for establishing a diagnosis of an allergy to coconut by detecting IgE antibodies in serum. It helps define the allergen responsible for eliciting signs and symptoms and identifies allergens responsible for allergic responses or anaphylactic episodes. It is used to confirm sensitization prior to immunotherapy and to investigate the specificity of allergic reactions to various allergens.
Special Instructions
Not provided.
Limitations
Testing for IgE antibodies is not useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists or in patients where medical management does not depend on identification of allergen specificity. False-positive results may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding to allergen solid phases.
FDA ApprovedNew York Approved
Methodology
Immunoassay (FEIA)
Biomarkers
Coconut, IgE
Analyte
LOINC Codes
- 6081-4 - Coconut IgE Qn
- 6081-4 - Coconut IgE Qn
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL for every 5 allergens requested
Minimum Volume
0.3 mL for 1 allergen
Container
Serum gel (preferred), Red top (acceptable), Submission in Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Causes for Rejection
Gross hemolysis: OK; Gross lipemia: OK
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |