Test Code C7 C7 Complement, Functional, Serum
Reporting Name
C7 Complement, Functional, SUseful For
Diagnosis of C7 deficiency
Investigation of a patient with an undetectable total complement level
Ordering Guidance
The total complement assay (COM / Complement, Total, Serum) assay should be used as a screen for suspected complement deficiencies before ordering individual complement component assays. A deficiency of an individual component of the complement cascade will result in an undetectable total complement level.
Specimen Required
Patient Preparation:
Fasting: 12 hours, preferred but not required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL serum
Collection Instructions:
1. Immediately after specimen collection, place the tube on wet ice and allow specimen to clot.
2. Centrifuge at 4° C and aliquot serum into a plastic vial.
3. Within 30 minutes of centrifugation, freeze specimen. Specimen must be placed on dry ice if not frozen immediately.
Note: If a refrigerated centrifuge is not available, it is acceptable to use a room temperature centrifuge, provided the sample is kept on ice before centrifugation, and immediately afterward, the serum is aliquoted and frozen.
Specimen Type
SerumSpecimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Frozen | 14 days |
Day(s) Performed
Tuesday, Friday
TAT: 3 - 5 days
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Method Name
Turbidimetric Measurement of Liposome Lysis
Method Description
Testing is performed on the Binding Site Optilite turbidimetric analyzer with the Optilite CH50 Reagent kit using modified manufacturer's instructions. C7 activity is measured by mixing patient serum with C7-deficient serum. The lytic activity of the serum mixture is tested against sensitized, labeled liposomes.(Package insert: Optilite CH50 Reagent, The Binding Site Group, Ltd.; INS095.OPTA, 08/2024)
Reference Values
≥ 58 U/mL
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
86161
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| C7FX | C7 Complement, Functional, S | 87724-1 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| C7FX | C7 Complement, Functional, S | 87724-1 |
Report Available
1 to 3 daysReject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | OK |