Test ID BLOD1207 Strongyloides Antibody, IgG, Serum
Reporting Name
Strongyloides Ab, IgG, SUseful For
Screening for the presence of IgG-class antibodies to Strongyloides
This test is not useful for monitoring patient response to therapy as IgG-class antibodies to Strongyloides may remain detectable following resolution of infection.
Specimen Type
SerumSpecimen 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) | 30 days | |
Frozen | 30 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Heat inactivated specimen | Reject |
Reference Values
Negative
Reference values apply to all ages.
Day(s) Performed
Monday, Wednesday, Thursday, Friday
Report Available
Same day/1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterMethod Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Testing Algorithm
For more information see Parasitic Investigation of Stool Specimens Algorithm.
Special Instructions
Secondary ID
63866CPT Code Information
86682
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.Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.
Sanford Interface Build Information
Result Code | Result Code Description |
---|---|
9611 | Strongyloides IgG Ab |