Epidermophyton floccosum IgE
Use
The Epidermophyton floccosum IgE test is used to detect the presence of specific IgE antibodies to the Epidermophyton floccosum antigen. This test is clinically significant in the evaluation of patients suspected of having an allergic reaction to this particular antigen. Allergy to Epidermophyton floccosum can manifest as skin rashes and other allergic symptoms upon exposure. This test aids in the diagnosis and management of such allergic conditions.
Special Instructions
This test can be ordered by New York State clients as it is approved for use in that state. Blood should be drawn in a plain red-top tube, although serum gel tubes are also acceptable. After draw, the sample should be spun down, and 0.5 mL of serum should be sent refrigerated in a plastic vial for optimal preservation.
Limitations
This test has not been cleared or approved by the U.S. Food and Drug Administration. Its performance characteristics have been determined by Eurofins Viracor. Testing is limited to the detection of IgE antibodies specific to Epidermophyton floccosum, and results may not account for the patient's complete allergy profile. Hemolysis, high lipemia, or improper sample handling can impact the test results.
New York Approved
Methodology
Immunoassay (ELISA)
Biomarkers
LOINC Codes
- 7307-2
- 7307-2
Result Turnaround Time
4-7 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.5 mL
Container
Red Top
Collection Instructions
Draw blood in a plain red-top tube, serum gel tube is acceptable. Spin down and send 0.5 mL of serum refrigerated in a plastic vial.
Causes for Rejection
Lipemia
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 28 days |
| Refrigerated | 28 days |
| Frozen | 365 days |