Clam, IgE, Serum
Use
This test is useful for establishing a diagnosis of an allergy to clam by identifying the allergen responsible for eliciting signs and symptoms. It helps in identifying allergens responsible for allergic responses or anaphylactic episodes and confirming sensitization prior to initiating immunotherapy. Additionally, it assists in investigating the specificity of allergic reactions, including those related to insect venom allergens, drugs, or chemical allergens.
Special Instructions
Not provided.
Limitations
Testing for IgE antibodies is not useful in patients previously treated with immunotherapy to determine residual clinical sensitivity or in cases where medical management doesn't require identification of allergen specificity. False-positive results can occur in patients with elevated serum IgE (>2500 kU/L) due to non-specific binding.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescence Enzyme Immunoassay (FEIA))
Biomarkers
LOINC Codes
- 6076-4 - Clam IgE Qn
- 6076-4 - Clam 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 >1 allergen: (0.05 mL x number of allergens) + 0.25 mL deadspace
Container
Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Storage Instructions
Refrigerated (preferred) for 14 days or frozen for 90 days
Causes for Rejection
Gross hemolysis and gross lipemia are acceptable
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |