Anti-MAG Neuropathy Plasma

Anti-MAG Neuropathy Plasma for Autoimmune Peripheral Nerve Research

Anti-MAG Neuropathy Plasma is collected from IRB-consented donors clinically diagnosed with anti-myelin-associated glycoprotein (anti-MAG) neuropathy and processed within one day of collection to preserve immunoglobulins, complement components, cytokines, and metabolites. Anti-MAG neuropathy is a genuinely autoantibody-mediated disorder, and plasma is the matrix in which its defining pathogenic antibody and downstream effector mechanisms are measured.

Anti-MAG Neuropathy Immunology and Why Plasma

  • The disease is defined by a monoclonal IgM antibody, usually of kappa light chain type, directed against myelin-associated glycoprotein – a glycoprotein of peripheral nerve myelin that shares the HNK-1 carbohydrate epitope with related glycoconjugates.
  • The IgM paraprotein almost always arises from an underlying IgM monoclonal gammopathy of undetermined significance, and less commonly from Waldenstrom macroglobulinaemia or another IgM-secreting lymphoproliferative disorder.
  • Anti-MAG IgM deposits on the outer myelin lamellae and fixes complement, producing the widely spaced myelin lamellae seen on nerve biopsy ultrastructure and driving demyelination.
  • The clinical phenotype is a slowly progressive, distal, sensory-predominant demyelinating polyneuropathy with prominent sensory ataxia and tremor – often described as distal acquired demyelinating symmetric (DADS) neuropathy – and distinguishing it from CIDP has direct therapeutic consequences.
  • High anti-MAG IgM titre supports the diagnosis and is the primary serological readout; treatment strategies target the antibody-producing B-cell clone, most commonly with anti-CD20 therapy such as rituximab.
  • Plasma is acellular and is the correct matrix for anti-MAG antibody titre, IgM paraprotein quantification, immunofixation, complement measurement, and neurofilament light chain. Cell-based B-cell work requires the paired PBMC product.

Donor Stratification Available

  • Anti-MAG IgM antibody titre where serological testing is documented
  • Underlying haematological context: IgM MGUS versus Waldenstrom macroglobulinaemia or other IgM lymphoproliferative disorder
  • Paraprotein isotype and light chain type where characterised
  • Clinical phenotype: sensory-predominant versus sensorimotor involvement, and presence of tremor or sensory ataxia
  • Treatment exposure: rituximab-naive versus anti-CD20 treated, or prior IVIg or plasma exchange
  • Disease duration and functional disability score where available
  • Matched healthy controls available

Product Features

  • Research Use Only (RUO)
  • Plasma collected from clinically confirmed anti-MAG neuropathy donors
  • Processed within one day of collection
  • Choice of anticoagulant on request
  • IRB-approved protocols and informed consent
  • Custom aliquot volumes available upon request

De-identified Donor Data

  • Verified anti-MAG neuropathy diagnosis
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Anti-MAG serology, paraprotein characterisation, and treatment history where documented
  • Additional anti-MAG neuropathy-specific metadata available on request

Applications

  • Anti-MAG antibody assay development, titre standardisation, and platform bridging
  • IgM paraprotein quantification, immunofixation, and free light chain analysis
  • Epitope mapping against MAG and HNK-1-bearing glycoconjugates
  • Complement activation product measurement as a downstream effector readout
  • Neurofilament light chain and other axonal damage marker measurement
  • Cytokine, chemokine, and B-cell survival factor profiling, including BAFF and APRIL
  • Pharmacodynamic monitoring of anti-CD20 and other B-cell-directed therapies
  • Differential biomarker discovery to separate anti-MAG neuropathy from CIDP and other demyelinating neuropathies

Other Anti-MAG Neuropathy Specimen Types

Compliance and Quality Assurance

  • IRB-approved and HIPAA-compliant protocols
  • Electronic informed consent with 21 CFR Part 11-compliant e-signatures
  • Documentation support available for regulatory review

Ordering & Customization

Anti-MAG neuropathy plasma is available in standard and custom volumes. For pricing, international orders, or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations. To compare donor availability across conditions, visit our human plasma page.

Protocols & Documentation

  • Plasma Isolation

    Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.

    Download
  • Informed Consent Form (ICF)

    Available upon request — confirms donor consent for research use and downstream commercialization.

Plasma

Frequently Asked Questions

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Are samples IRB approved?

1 Answer

YES – All collections are conducted under IRB-approved protocols and electronic informed consent. Sanguine utilizes Advarra and WCG IRB for oversight.

YES – all our products are research use only (RUO).

Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.

Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.

Sanguine offers flexible prospective collection services tailored to fit your research. For more information and to request a quote, please see: our prospective biospecimen collection services page.

Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.

YES – we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.

Each sample from a different individual – Unique donor means each sample comes from a different person, ensuring biological diversity in your study.

YES – Unique donors can be specified and guaranteed based on your requirements.

For information about sample quality, please see: Quality and Compliance

YES – “IRB-approved collection protocols” and IRB approval documentation available upon request. Sanguine utilizes two internationally-recognized IRBs (Advarra and WCG IRB) for review and approval.

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Need a custom Plasma cohort?

Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.

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