Order Code TXPG Toxoplasma gondii Antibody, IgG, Serum
Ordering Guidance
IgG antibodies in patients younger than 6 months of age are typically the result of passive transfer from the mother. To assess possible Toxoplasma gondii infection in patients younger than 6 months, order TXPM / Toxoplasma gondii Antibody, IgM, Serum.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.6 mL
Collection Instructions: Centrifuge and aliquot serum into plastic vial
Useful For
Quantitative detection of IgG antibodies to Toxoplasma gondii.
This test is not useful for diagnosing infection in infants younger than 6 months of age. In that age group, IgG antibodies usually are the result of passive transfer from the mother.
Method Name
Electrochemiluminescence Immunoassay (ECLIA)
Reporting Name
Toxoplasma Ab, IgG, SSpecimen Type
SerumSpecimen Minimum Volume
0.6 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 21 days |
| Frozen | 90 days | |
| Ambient | 72 hours |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
| Additives (eg, biocides, antioxidants) | Reject |
Reference Values
Negative
<1 IU/mL Negative
≥1-<3 IU/mL Borderline
≥3 IU/mL Positive
Reference values apply to all ages.
Method Description
The electrochemiluminescence immunoassay for the in vitro quantitative determination of IgG antibodies to Toxoplasma gondii in human serum is a sandwich test principle. During the first incubation, 6 mcL of sample a biotinylated recombinant T. gondii-specific antigen labeled with a ruthenium complex form a sandwich complex. In the second incubation, streptavidin-coated microparticles are added and the complex becomes bound to the solid phase via interaction of biotin and streptavidin. The reaction mixture is aspirated into the measuring cell where the microparticles are magnetically captured onto the surface of the electrode. Unbound substances are then removed with ProCell II M. Application of a voltage to the electrode then induces chemiluminescent emission which is measured by a photomultiplier. Results are determined by a calibration curve which is instrument-specifically generated by 2-point calibration and a master curve provided via the cobas link.(Package insert: Elecsys Toxo IgG, Roche Diagnostics GmbH, 02/2022)
Day(s) Performed
Monday through Saturday
Performing Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
86777
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| TXPG | Toxoplasma Ab, IgG, S | 8039-0 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| GTXP | Toxoplasma Ab, IgG, S | 40677-7 |
| DEX04 | Toxoplasma IgG Value | 8039-0 |