Allergen, Tree, Mulberry Red IgE
Also known as: MULBERRY
Use
This test measures the concentration of IgE antibodies specific to Mulberry Red Tree allergens in serum, using a quantitative method. It is intended to aid in the diagnosis of IgE-mediated allergic conditions. The clinical relevance of results in the range of 0.10-0.34 kU/L is undetermined and requires specialist input. In this range, although the IgE level is increasing, it may not correlate with clinical reactions or skin test results when exposed to the allergen.
Special Instructions
Not provided.
Limitations
Allergen results within the range of 0.10-0.34 kU/L may not necessarily correlate with clinical allergies or anaphylaxis. Even results at higher concentrations might not mirror the degree of clinical response to the Mulberry Red Tree allergens in practical exposure scenarios. Thus, correlation with clinical history and in vivo reactivity is essential. This test has not been cleared or approved by the FDA and is intended for clinical purposes in a CLIA certified laboratory setting.
New York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
Mulberry Red IgE
Analyte
LOINC Codes
- 7514-3 - Red mulberry 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. Transfer required volume to the specified transport tube.
Patient Preparation
Multiple patient encounters should be avoided.
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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