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Test Code C1QM C1q Complement, Functional, Serum

Additional Codes

MAYO Test ID
C1QFX
EPIC Test ID
LAB2373

 

Reporting Name

C1Q Complement, Functional, S

Useful For

Diagnosis of C1 deficiency

 

Investigation of a patient with an absent total complement level

Method Name

Automated Liposome Lysis Assay

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Serum


Ordering Guidance


The total complement assay (COM / Complement, Total, Serum) 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 preferred

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

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. Sample 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 specimen is kept on ice before centrifugation, and immediately afterward, the serum aliquoted and frozen.


Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Frozen 14 days

Reject Due To

Gross hemolysis OK
Gross lipemia Reject
Gross icterus OK

Reference Values

34-63 U/mL

Day(s) Performed

Monday through Friday

CPT Code Information

86161

LOINC Code Information

Test ID Test Order Name Order LOINC Value
C1QFX C1Q Complement, Functional, S 87722-5

 

Result ID Test Result Name Result LOINC Value
C1QFX C1Q Complement, Functional, S 87722-5

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.

Report Available

1 to 3 days