Test Code TOXGP Toxoplasma gondii Antibody, IgG, Serum
Reporting Name
Toxoplasma Ab, IgG, SUseful For
Determining whether a patient has had previous exposure to or recent infection with 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.
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
SerumOrdering 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 TXM / Toxoplasma gondii Antibody, IgM, Serum.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Minimum Volume
0.4 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 14 days | |
Frozen | 14 days |
Reference Values
Toxoplasma ANTIBODY, IgG
Negative
Toxoplasma IgG
≤9 IU/mL (Negative)
10-11 IU/mL (Equivocal)
≥12 IU/mL (Positive)
Reference values apply to all ages.
Day(s) Performed
Monday through Saturday
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86777
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
TOXGP | Toxoplasma Ab, IgG, S | 88746-3 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
TOXG | Toxoplasma Ab, IgG, S | 40677-7 |
DEXG6 | Toxoplasma IgG Value | 8039-0 |
Method Description
The BioPlex 2200 Toxoplasma IgG assay uses multiplex flow immunoassay technology. Briefly, Toxoplasma antigen-coated fluorescent beads are mixed with an aliquot of patient sample and sample diluent and incubated at 37° C. During this time, IgG anti-Toxoplasma antibodies in the specimen bind to the Toxoplasma antigen on the beads. After a wash cycle, a fluorescently-labeled antihuman IgG-antibody conjugate is added to the mixture and incubated at 37° C. Following a wash step to remove unbound conjugate, the bead mixture is passed through a detector that identifies the bead based on dye fluorescence and determines the amount of antibody captured by the antigen based on fluorescence of the antihuman IgG conjugate. Raw data is calculated in relative fluorescence intensity and converted to an antibody index for interpretation.
Three additional dyed beads, an internal standard bead, a serum verification bead, and a reagent black bead are present in each reaction mixture to verify detector response, the addition of serum to the reaction vessel, and the absence of significant nonspecific binding in serum, respectively.(Package insert: BioPlex 2200 System, ToRC IgG. Bio-Rad Laboratories; 03/2012)
Report Available
Same day/1 to 3 daysReject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Heat-inactivated specimen | Reject |
Method Name
Multiplex Flow Immunoassay (MFI)
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.