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Test ID FINA NAbFeron (IFNB-1) Neutralizing Antibody Test

Method Name

Viral Cytopathic Effect Assay

Reporting Name

NAbFeron (IFN-B) Antibody

Specimen Type

Serum


Specimen Required


Patient Preparation: Specimen should be collected either before treatment with interferon or more than 24 hours following the most recent dose. Patient should not be on steroid therapy for at least two weeks prior to testing.

Collection Container/Tube: Red top or serum gel

Submission Container/Tube: Plastic vial

Specimen Volume: 2 mL serum

Collection Instructions:

1. Within 48 hours of collection, centrifuge and aliquot 2 mL of serum into a plastic vial.

2. Send refrigerate.


Specimen Minimum Volume

Serum: 0.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 28 days
  Frozen  180 days
  Ambient  72 hours

Reference Values

<1:20

Day(s) Performed

Monday through Friday

Performing Laboratory

Athena Diagnostics

CPT Code Information

86382

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FINA NAbFeron (IFN-B) Antibody Not Provided

 

Result ID Test Result Name Result LOINC Value
Z0083 NAbFeron (IFN-B) Antibody Not Provided

Test Classification

This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by U.S. Food and Drug Administration. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes. .

Report Available

14 to 25 days

NY State Approved

Yes