Plaice, IgE, Serum
Use
The Plaice, IgE, Serum test is useful for establishing a diagnosis of an allergy to plaice and defining the allergen responsible for eliciting signs and symptoms. It also aids in identifying allergens responsible for allergic responses and/or anaphylactic episodes and is used to confirm sensitization prior to beginning immunotherapy. This test isn't useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists, or in cases where medical management doesn't rely on allergen specificity.
Special Instructions
Not provided.
Limitations
Some individuals with clinically insignificant sensitivity to allergens may still have measurable levels of IgE antibodies, and results must be interpreted clinically. 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
IgE
Protein
LOINC Codes
- 10959-5 - Plaice IgE Qn
- 10959-5 - Plaice 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
For 1 allergen: 0.3 mL
Container
Preferred: Serum gel, Acceptable: Red top
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |