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2013890
Toxoplasma gondii Antibody, IgA by ELISA, Serum
TOXOG IGA
Ordering Recommendation
Use only in neonates for cases of suspected congenital toxoplasmosis.
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Plain red or serum separator tube (SST).
Specimen Preparation
Transfer 3 mL serum to an ARUP standard transport tube. (Min: 0.5 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.
Storage/Transport Temperature
Refrigerated. Also acceptable: Frozen.
Unacceptable Conditions
Grossly hemolyzed, icteric, lipemic, and bacterially contaminated specimens.
Remarks
Stability
Ambient: Undefined; Refrigerated: 1 week; Frozen: Indefinitely
Methodology
Semi-Quantitative Enzyme-Linked Immunosorbent Assay (ELISA)
Performed
Varies
Reported
5-12 days
Reference Interval
By Report
Interpretive Data
Compliance Category
Performed by non-ARUP Laboratory
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
86777
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2013891 | Toxoplasma gondii Ab, IgA, ELISA, Serum | 10723-5 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
Toxoplasma gondii Antibody, IgA by ELISA, Serum
PAMF Remington Laboratory
