Acarus siro, IgE, Serum
Use
Establishing the diagnosis of an allergy to Acarus siro (flour mites) and defining the allergen responsible for eliciting signs and symptoms. It aids in identifying allergens responsible for allergic response and/or anaphylactic episode, confirming sensitization prior to immunotherapy, and investigating the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens. Useful for understanding the patient’s allergic profile and directing appropriate therapeutic interventions.
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 whose medical management does not depend upon identification of allergen specificity. False-positive results for IgE may occur in patients with elevated serum IgE due to nonspecific binding. Some individuals might show measurable levels of IgE antibodies despite clinically insignificant sensitivity.
FDA ApprovedNew York Approved
Methodology
Immunoassay (FEIA)
Biomarkers
Acarus siro
Protein
LOINC Codes
- 6254-7 - A siro IgE Qn
- 6254-7 - A siro 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
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
Gross hemolysis: OK, Gross lipemia: OK
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |