Bovine Serum Albumin, IgE, Serum
Use
This test is useful for establishing the diagnosis of an allergy to bovine serum albumin, defining the allergen responsible for eliciting signs and symptoms, identifying allergens responsible for allergic response or anaphylactic episodes, confirming sensitization prior to immunotherapy, and investigating the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens. The presence of IgE antibodies in serum increases the likelihood of allergic disease, while also indicating potential allergens causing symptoms.
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, nor is it useful in patients whose medical management does not depend upon identification of allergen specificity. False-positive results can occur in patients with elevated serum IgE (>2500 kU/L) due to nonspecific binding.
New York Approved
Methodology
Immunoassay (Fluorescence Enzyme Immunoassay (FEIA))
Biomarkers
Bovine Serum Albumin
Protein
LOINC Codes
- 10922-3 - BSA IgE Qn
- 10922-3 - BSA 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
Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Causes for Rejection
None
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |