Overview +

All Sanguine study protocols and their resulting samples, which include all Sanguine at-home and apheresis collection programs, are conducted under an Institutional Review Board (IRB). Sanguine operates under an electronic informed consent process which executes 21 CFR part 11 compliant e-signatures, and Sanguine systems interacting with study participant information are HIPAA-compliant.

Sanguine’s human serum is isolated with precision to ensure high purity and reliability for research and therapeutic applications. Collected from whole blood, our serum is carefully isolated and cryopreserved within one day to preserve the integrity of essential biomarkers. Serum include verified diagnosis for disease state, and donor-reported allergies and infectious disease history.

Well-characterized serum for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) research supports studies on neuroinflammation, genetic mutations, and potential therapies to advance understanding and treatment of this rare neurodegenerative disorder.

Infectious disease testing requirements differ globally. If you are ordering from outside the U.S., please reach out at to confirm that we can meet your country’s regulatory and documentation needs.

Protocol and Documentation +

Document Type Technical Document Catalog Language
PDF > Leukopak Cryopreservation - -
PDF > Leukopak Thawing - -

Data and Testing +

Data and Testing with Every Sample

  • Donor demographics
  • Donor-reported allergies
  • Donor-reported infectious disease history

Compliance & Quality Assured

For quality and compliance related information, please visit Sanguine quality and compliance page.

For privacy related information, please visit Sanguine privacy policy page.