Bordetella pertussis Antibody, IgM by Immunoblot
New York DOH Approval Status
Serum separator tube.
Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.15 mL)
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Effective February 19, 2013
|Bordetella pertussis Antibody, IgM by Immunoblot|
|Bordetella pertussis Ab, IgM by Immunoblot Interp||Negative|
|B. pertussis, IgM Immunoblot PT||Negative|
|B. pertussis, IgM Immunoblot FHA||Negative|
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
This assay tests for the presence of pertussis toxin (PT) and filamentous hemagglutinin antibody (FHA).
|Component Test Code*||Component Chart Name||LOINC|
|2004323||B. pertussis Ab, IgM Immunoblot Interp||50398-7|
|2004324||B. pertussis, IgM Immunoblot FHA||43882-0|
|2004325||B. pertussis, IgM Immunoblot PT|
- B. pertussis IgM immunoblot
- Pertussis Antibody
- Pertussis IgM Ab Immunoblot