Toxoplasma gondii, Amniotic Fluid, PCR
Use
This test is intended to be used in conjunction with standard serological tests to aid in the diagnosis of infections caused by Toxoplasma gondii.
Special Instructions
Not provided.
Limitations
This test was developed and its performance characteristics determined by LabCorp Laboratories. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This test is used for clinical purposes and should not be regarded as investigational or research.
Methodology
PCR-based (Real-time PCR)
Biomarkers
Toxoplasma gondii
Microorganism
LOINC Codes
- 27999-2 - T gondii DNA Amn Ql NAA+probe
- 27999-2 - T gondii DNA Amn Ql NAA+probe
Result Turnaround Time
4-6 days
Related Documents
For more information, please review the documents below
Specimen
Amniotic Fluid
Volume
0.5 mL
Minimum Volume
0.2 mL
Container
Sterile container
Collection Instructions
To avoid delays in turnaround time when requesting multiple tests on frozen samples, please submit separate frozen specimens for each test requested.
Storage Instructions
Freeze (preferred) or refrigerate.
Causes for Rejection
Quantity not sufficient for analysis; gross specimen contamination; specimen too old; leaking or broken tube
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 7 days |
| Frozen | 90 days |
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