Test Code IGD Immunoglobulin D (IgD), Serum
Additional Codes
| Epic Ordering Code | LAB5082 |
| NBS code | LBC12435 |
| Service code | 31941 |
Reporting Name
Immunoglobulin D (IgD), SSpecimen Type
SerumOrdering Guidance
To distinguish between polyclonal and monoclonal IgD, order IFXED / Immunofixation Heavy Chain Type Delta and Epsilon, Serum.
Specimen Required
Patient Preparation:
Fasting: 8 hours, preferred but not required
Supplies: Sarstedt 5 mL Aliquot Tube (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Specimen Volume: 1 mL serum
Collection Instructions: Centrifuge and aliquot serum into plastic vial.
NUH Outreach Laboratories:
Specimen Requirements
Submit only one of the following:
Preferred: Yellow Top
Acceptable: Red Top
Fasting: 8 hours, preferred but not required
Processing Requirements
Centrifuge and aliquot serum into a Mayo plastic tube.
Specimen type: Serum
Volume: 1 mL
Storage/transport requirements: Refrigerated
Specimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 28 days |
| Frozen | 28 days | |
| Ambient | 21 days |
Reject Due To
| Gross hemolysis | OK |
| Gross lipemia | Reject |
| Gross icterus | OK |
| Heat-activated specimen | Reject |
Method Name
Turbidimetry
Day(s) Performed
Monday through Friday
Report Available
1 to 3 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
≤10 mg/dL
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Providing information on the humoral immune status
Identifying an IgD monoclonal gammopathy
CPT Code Information
82784
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| IGD | Immunoglobulin D (IgD), S | 2460-4 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| IGD | Immunoglobulin D (IgD), S | 2460-4 |
Secondary ID
9272Test 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 31/07/2026