Test ID NSYPH Syphilis IgG Enzyme Immunoassay, Serum
Specimen Required
Collection Container/Tube: 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
An aid in the diagnosis of infection with Treponema pallidum
Routine prenatal screening
This test is not useful for diagnosis of congenital syphilis.
This test is not offered as a screening or confirmatory test for blood donor specimens.
Method Name
Enzyme Immunoassay (EIA)
Reporting Name
Syphilis IgG EIA, SSpecimen Type
SerumSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Frozen | 14 days |
Reference Values
Nonreactive
Reference values apply to all ages
Day(s) Performed
Monday through Friday, Sunday
Report Available
Same day/1 to 3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
86780
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
NSYPH | Syphilis IgG EIA, S | 47238-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
NSYPH | Syphilis IgG EIA, S | 47238-1 |
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.