Allergen, Weed, Kochia/Firebush
Also known as: KOCHIA
Use
This test is designed to measure allergen-specific IgE antibodies against the weed Kochia, also known as Firebush. Detecting these antibodies can help in diagnosing allergic responses related to this specific allergen. The results assist healthcare providers in the evaluation of allergic conditions and may be correlated with clinical history and in vivo reactivity to Kochia as part of a comprehensive allergy assessment.
Special Instructions
Not provided.
Limitations
The concentrations of allergen-specific IgE detected by this test may not directly correlate with the severity of a patient's clinical allergy symptoms or skin test responses. A negative test result does not definitively rule out the possibility of a clinical allergy or even anaphylaxis. Allergen results in the range of 0.10-0.34 kU/L have undetermined clinical relevance and should be interpreted in the context of a specialist's evaluation.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
LOINC Codes
- 6118-4 - Firebush 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 as soon as possible or within two hours of collection. Transfer to an ARUP Standard Transport Tube.
Patient Preparation
Multiple patient encounters should be avoided.
Storage Instructions
Refrigerate the specimen during storage and transport.
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens are unacceptable.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
Other tests from different labs that may be relevant