Soybean, IgE, Serum
Use
This test is useful for establishing a diagnosis of an allergy to soybean and defining the allergen responsible for eliciting signs and symptoms. It can identify allergens responsible for allergic responses and/or anaphylactic episodes, confirm sensitization before beginning immunotherapy, and investigate the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens. It is not useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists or in cases where medical management does not depend on allergen specificity.
Special Instructions
Not provided.
Limitations
Some individuals with clinically insignificant sensitivity to allergens may have measurable levels of IgE antibodies in serum, necessitating interpretation in a clinical context. False positives may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding. Testing for IgE antibodies is not useful in patients in whom medical management does not depend on identification of allergen specificity.
FDA ApprovedNew York Approved
Methodology
Immunoassay (FEIA)
Biomarkers
IgE
Analyte
LOINC Codes
- 6248-9 - Soybean IgE Qn
- 6248-9 - Soybean 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; For more than 1 allergen: (0.05 mL x number of allergens) + 0.25 mL deadspace
Container
Preferred: Serum gel; Acceptable: Red top; Submission: Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Storage Instructions
Refrigerated (preferred): 14 days; Frozen: 90 days.
Causes for Rejection
None specified for gross hemolysis or gross lipemia
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |