Casandra
Casandra Test Code QD96738Version 1 (DRAFT)
Performing Lab
Toxoplasma gondii (IgA) Antibody, ELISA
Clinical Use
Order TestUse
IgA antibodies against Toxoplasma gondii are detected in acute toxoplasmosis and are valuable for early detection of acute disease in pregnant women and individuals with AIDS; IgA antibodies do not cross the placenta and thus are reliable markers for congenital T. gondii infection.
Special Instructions
Not provided.
Limitations
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Test Details
Methodology
Immunoassay (ELISA)
Biomarkers
Toxoplasma gondii IgA antibody
AnalyteIgA Antibody • Concentration / Level • Quantitative (Continuous) (e.g., copies/mL, % expression)
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Serum
Volume
1 mL
Minimum Volume
0.1 mL
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 14 days |
| Frozen | 30 days |
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