Allergen, Fungi and Molds, Aureobasidium pullulans
Also known as: AUREOBASID
Use
This test measures the level of IgE antibodies specific to the mold Aureobasidium pullulans in a patient's serum. These IgE levels can help diagnose allergic reactions associated with exposure to this mold, which can cause respiratory issues and other allergy symptoms. The results can assist healthcare providers in assessing the presence and intensity of an allergic reaction to Aureobasidium pullulans.
Special Instructions
Not provided.
Limitations
The test results reflect the concentration of allergen-specific IgE but do not necessarily correlate with the severity of clinical symptoms or skin test results. The correlation between laboratory results and clinical history or in vivo reactivity is essential. A negative result does not exclude the possibility of allergy or anaphylaxis.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
Aureobasidium pullulans IgE
Protein
LOINC Codes
- 6029-3 - A pullulans IgE Qn
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.25 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Separate serum from cells ASAP or within 2 hours of collection.
Patient Preparation
Multiple patient encounters should be avoided.
Storage Instructions
Store refrigerated.
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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