Mint (Mentha Piperita) IgE
Use
This test measures IgE antibodies specific to mint (Mentha piperita) allergens in the serum. It is used to detect IgE mediated sensitization related to mint and cross-reactive species like peppermint and spearmint. The test helps in the diagnosis of allergic reactions to mint, which can be relevant for patients experiencing allergic symptoms after ingestion or exposure to substances containing mint.
Special Instructions
Specimen collection involves drawing blood in a red-top tube or a serum gel tube. Upon spinning and separating, a minimum volume of 0.5 mL serum is required for analysis. Ensure proper refrigeration for transport to maintain specimen integrity. Test ordering is available for New York State clients.
Limitations
The test has not been cleared or approved by the U.S. Food and Drug Administration and should be considered carefully in clinical interpretation. Results depend heavily on the quality of the specimen and the method's ability to detect specific IgE levels accurately. Mild hemolysis, lipemia, or icterus may not necessarily lead to specimen rejection, but gross instances will. Timing and proper handling conditions of the specimen are crucial to prevent inaccurate results.
New York Approved
Methodology
Immunoassay (ImmunoCAP FEIA)
Biomarkers
LOINC Codes
- 11190-6
- 11190-6
- 102445-4
Result Turnaround Time
1-6 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.5 mL
Container
Serum gel tube or plain red-top tube
Collection Instructions
Draw blood in a plain red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 0.5 mL of serum refrigerated in a plastic vial.
Storage Instructions
Refrigerate the sample; can also be stored ambient or frozen if needed.
Causes for Rejection
Gross hemolysis, lipemia, or icterus
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 28 days |
| Refrigerated | 28 days |
| Frozen | 365 days |