Ganglioside GD1a Antibody (IgG), EIA

Ganglioside GD1a Antibody (IgG), EIA

Test Code

38916
83520
38916
83520
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Ganglioside GD1a Antibody (IgG), EIA - Ganglioside GD1a antibody IgG is associated with acute motor axonal neuropathy, sometimes followed by Campylobacter jejuni infections. Ganglioside GD1a antibody IgG can aid in the diagnosis of acute motor axonal neuropathy variant of Guillain-Barre syndrome.

Test Resources

None found for this test
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Test Details

Patient Preparation

Overnite fasting is preferred

Methodology

Enzyme Immunoassay (EIA)

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest 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.

Reference Range(s)

<1:100 titer

LOINC® Codes, Performing Laboratory

Overnite fasting is preferred

Methodology

Enzyme Immunoassay (EIA)
This test was developed and its analytical performance characteristics have been determined by Quest 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.

Reference Range(s)

<1:100 titer

Preferred Specimen(s)

1 mL serum

Minimum Volume

0.2 mL

Transport Container

Transport tube

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 7 days
  • Frozen: 30 Days

Reject Criteria

Received room temperature

Setup Schedule

1 mL serum
0.2 mL
Transport tube
Refrigerated (cold packs)
Room temperature: 24 hours
Refrigerated: 7 days
Frozen: 30 Days
Received room temperature
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

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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