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Test Code IGERAB IgE Receptor Antibody

Important Note

Mayo Test Code FGERA


Specimen Required


Container/Tube:

Preferred: Red top tube

Acceptable: Serum gel tube

Specimen Volume: 1.0 mL

Collection Instructions: Draw blood in a plain, red-top tube(s) or serum gel tube(s). Separate serum from cells immediately by centrifugation and aliquot into a polypropylene or similar plastic tube. Send 1 mL of serum frozen in plastic vial.

 

Complete and submit with specimen:

1. National Jewish Immunology Diagnostics request form.

2. Patient's date of birth is required on the National Jewish Immunology Diagnostics request form


Useful For

The test detects functional autoantibodies to the Fc-epsilon receptor (high affinity IgE receptor) or to IgE and is useful in the evaluation of chronic urticaria.

Method Name

Flow Cytometry

Reporting Name

IgE Receptor Antibody

Specimen Type

Serum

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Frozen (preferred) 365 days
  Refrigerated  7 days
  Ambient  48 hours

Reference Values

0 - 12

Day(s) and Time(s) Performed

Monday, Thursday

Analytic Time

7 - 9 days

Performing Laboratory

National Jewish Health

Test Classification

This test uses a kit/reagent designated by the manufacturer as "for research use, not for clinical use" as well as one or more reagents classified as an analyte specific reagent (ASR). The performance characteristics of this test have been validated by Advanced Diagnostic Laboratories at National Jewish Health. It has not been cleared or approved by the US Food and Drug Administration. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. This laboratory is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA-88) as qualified to perform high complexity clinical laboratory testing.

CPT Code Information

88184

88185 x 2

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FGERA IgE Receptor Antibody In Process

 

Result ID Test Result Name Result LOINC Value
Z5123 Basophils (%), CD203c In Process
Z5124 Interpretation: In Process

NY State Approved

Yes
Northwell Health Laboratories Additional Information:

Computer Interface Code

   PDM #  5905820