Bumblebee
Also known as: Venom
Use
The Bumblebee test is specifically designed to measure specific IgE antibodies to bumblebee venom. It is useful in diagnosing allergic reactions to bumblebee stings and can help guide management of patients with such allergies. Levels of specific IgE provide insight into the likelihood of an allergic response and can aid in determining the necessity of immunotherapy or avoidance strategies.
Special Instructions
This test utilizes the Thermo Fisher ImmunoCAP methodology, known for its sensitivity in detecting specific IgE antibodies. It is critical for clinicians to ensure proper specimen collection and handling as per the guidelines provided.
Limitations
False positives or false negatives can occur and may be influenced by various factors including cross-reactivity with other allergens or low levels of specific IgE. Interpretation of results should be done in conjunction with a clinical evaluation and patient history. This test may not provide exhaustive information on all possible bumblebee venom allergens.
Methodology
Immunoassay (CLIA)
Biomarkers
LOINC Codes
- 6056-6
- 6056-6
Result Turnaround Time
3-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.2 mL
Minimum Volume
Not provided
Container
Red-top tube or gel-barrier tube
Storage Instructions
Room temperature
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 14 days |
| Refrigerated | 14 days |
| Frozen | 3 months |
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