Test Code C1ES C1 Esterase Inhibitor Antigen, Serum
Additional Codes
| Epic Ordering Code | LAB3040936 |
| NBS code | LBC13318 |
| Service code | 36934 |
Reporting Name
C1 Esterase Inhibitor Antigen, SSpecimen Type
SerumSpecimen Required
Patient Preparations:
Fasting: 12 hours, preferred but not required.
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Immediately after specimen collection, place the tube on wet ice.
2. Centrifuge and aliquot serum into plastic vial.
3. Freeze specimen within 30 minutes.
NUH Outreach Laboratories:
Specimen Requirements
Submit only one of the following:
Preferred: Red Top
Acceptable: Gold Top
Processing Requirements
Centrifuge and aliquot serum into a plastic vial.
Specimen type: Serum
Volume: 1 mL
Storage/transport requirements: Refrigerated
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Frozen (preferred) | 28 days |
| Refrigerated | 28 days | |
| Ambient | 72 hours |
Reject Due To
| Gross hemolysis | OK |
| Gross lipemia | Reject |
| Gross icterus | OK |
Method Name
Nephelometry
Day(s) Performed
Monday through Friday
Report Available
2 to 5 daysPlease note that this is a referral test requiring transport to the external testing facility and an additional 3-5 days is required.
Reference Values
19-37 mg/dL
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Diagnosis of hereditary angioedema
Monitoring levels of C1 esterase inhibitor in response to therapy
CPT Code Information
83883
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| C1ES | C1 Esterase Inhibitor Antigen, S | 4477-6 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| C1ES | C1 Esterase Inhibitor Antigen, S | 4477-6 |
Secondary ID
8198Test 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.Last updated 03/07/2026