SensoriMotor Neuropathy Profile with Recombx®-Complete
Test code
CPT code(s)*
Details
Includes
Co-GM1 Autoantibody Test
Co-Asialo-GM1 Autoantibody Test
Co-GD1b Autoantibody Test
GD1a Autoantibody Test
GALOP Autoantibody Test
SGPG Autoantibody Test
MAG Autoantibody Test
Recombx® Hu Autoantibody Test
Sulfatide Autoantibody Test
Methodology
Automated Nanoliter Scale Immunoassay • Enzyme Linked Immunosorbent Assay (ELISA) • Western Blot (WB)
Assay category
This test was developed and its analytical performance characteristics have been determined by Athena Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Alternative name(s)
ANNA-1
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 2 mL serum |
| Minimum volume | 0.5 mL |
| Collection instructions | Serum must be separated from cells within 48 hours of collection. Note: Please label each specimen tube with two forms of patient identification. These forms of identification must also appear on the requisition form. |
| Transport container | Transport tube |
| Transport temperature | Refrigerated (cold packs) |
| Specimen stability | Room temperature: 72 hours Refrigerated: 21 days Frozen: 28 days |
| Reject criteria | Hemolysis • Lipemia • Icteric |
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
*The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.
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