Anti-MAG Neuropathy Plasma
Anti-MAG Neuropathy Plasma from donors with clinically confirmed IgM anti-myelin-associated glycoprotein autoimmune neuropathy. Useful for anti-MAG antibody titre and assay development, IgM paraprotein quantification, complement activation products, neurofilament light chain, and monitoring of B-cell-directed therapy. Matched healthy controls available.
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
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Download
Plasma Isolation
Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Plasma
Frequently Asked Questions
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YES – All collections are conducted under IRB-approved protocols and electronic informed consent. Sanguine utilizes Advarra and WCG IRB for oversight.
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YES – all our products are research use only (RUO).
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You can find our full product catalog here.
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Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.
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Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.
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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.
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Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.
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YES – we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.
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Each sample from a different individual – Unique donor means each sample comes from a different person, ensuring biological diversity in your study.
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YES – Unique donors can be specified and guaranteed based on your requirements.
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For information about sample quality, please see: Quality and Compliance
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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.