APECED Plasma

APECED Plasma | Human Plasma from Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Donors

APECED Plasma is collected from donors clinically diagnosed with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED, also known as APS-1) and processed within hours of collection to preserve key analytes such as cytokines, proteins, and metabolites. APECED is caused by biallelic AIRE mutations that break central immune tolerance, producing the characteristic triad of hypoparathyroidism, adrenal insufficiency, and chronic mucocutaneous candidiasis, along with high-titre anti-interferon-ω and anti-IL-22 autoantibodies. This human plasma supports research focused on endocrine dysfunction, autoantibody profiling, and APECED therapeutic development.

Product Features

  • Research Use Only (RUO)
  • APECED plasma collected from clinically confirmed APECED donors
  • Processed within one day of collection
  • IRB-approved protocols and informed consent
  • Custom aliquot volumes available upon request

De-identified Donor Data

  • Verified Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) diagnosis
  • AIRE genotype where available
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Additional APECED-specific metadata available

Applications

  • Anti-interferon-ω and anti-IL-22 autoantibody profiling
  • Biomarker discovery and validation
  • Cytokine and inflammation profiling
  • Metabolomics and proteomics studies
  • Therapeutic response research

Other APECED Specimen Types

APECED donor material is also available as APECED PBMC, APECED serum, and APECED whole blood. If you need an APECED leukopak or another apheresis-derived cell product, we can arrange a custom collection — see our human leukopak page for specifications and current availability, or contact us to scope a disease-specific leukopak draw.

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 and Customization

APECED plasma is available in standard and custom volumes. For international orders or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations. For the full specimen range, see our human plasma collection.

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.

More Information