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Test ID FMYOP MyoMarker Panel 2

Method Name

RIPA and Enzyme Immunoassay (EIA)

Reporting Name

MyoMarker Panel 2

Specimen Type

Varies

Submit only 1 of the following specimens:

 

Serum

Draw blood in a plain, red-top tube(s), serum gel tube(s) is acceptable. Spin down and send 3 mL of serum refrigerate in plastic vial.

 

Plasma

Draw blood in a lavender-top (EDTA) tube(s). Spin down and send 3 mL of EDTA plasma refrigerate in plastic vial.

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated (preferred) 7 days
  Frozen  180 days
  Ambient  7 days

Clinical Information

1.  Anti-Jo 1 Abs are found in subset of myositis patients characterized by interstitial lung disease, systemic polyarthritis, Raynaud’s Phenomena, fever and Mechanic’s Hand (anti-synthetase syndrome).

2.  Anti-Jo 1 appears to be a marker for interstitial lung disease in polymyositis.

 

Reference Values

Mi-2, PL-12, PL-7, EJ, OJ, SRP, Ku, U2 snRNP

 

Reference Range:  Negative

 

Anti-PM/Scl Ab, Anti-Jo-1 Ab

 

Reference Range: <20

 

EIA Interpretation:

 

Negative:                      <20 units

Weak Positive:              20 – 39 units

Moderate Positive:        40 – 80 units

Strong Positive:            >80 units

Day(s) Performed

Batched weekly

Report Available

10 - 14 days

Performing Laboratory

RDL Reference Laboratory, Inc.

Test Classification

This panel was developed and its performance characteristics validated by RDL. There is no FDA approved assay for the above tests. As a lab developed test (LDT), approval or clearance by the FDA is not required. This test may be used for clinical purposes and should not be regarded as investigational or for research.

CPT Code Information

83516/Mi-2

83516/PL-12

83516/PL-7

83516/EJ

83516/OJ

83516/SRP

83516/Ku

83516/U2 snRNP

83516/Anti-PM/Scl Ab

86235/Anti-Jo 1 Ab

 

NY State Approved

Yes