Myasthenia Gravis Bulk Plasma

About Myasthenia Gravis Bulk Plasma

Myasthenia Gravis Bulk Plasma Collected via Apheresis in ACDA

Myasthenia Gravis Plasma is collected from IRB-consented donors diagnosed with Myasthenia Gravis, using apheresis and ACDA (Acid-Citrate-Dextrose Formula A) as the anticoagulant. This disease-state plasma supports immunological and biomarker research and is ideal for assay development and therapeutic discovery.

Product Features

  • High-volume plasma collected via apheresis
  • Anticoagulated using ACDA
  • Tested and confirmed negative for HIV, HBV, and HCV
  • Available fresh with custom volumes upon request
  • IRB-approved informed consent and HIPAA-compliant handling

De-identified Donor Data

  • Clinically confirmed diagnosis of Myasthenia Gravis
  • Donor demographics: age, sex assigned at birth, race/ethnicity
  • Clinical history and medication data available

Applications

  • Disease-specific biomarker discovery
  • Inflammatory and immunological assay development
  • Proteomic, metabolomic, and cytokine profiling
  • Therapeutic development and validation studies

Compliance and Quality Assurance

  • Screened negative for HIV, HBV, and HCV
  • IRB-approved collection with 21 CFR Part 11–compliant consent
  • Standardized processing and cryopreservation protocols

Ordering & Customization

Myasthenia Gravis Bulk Plasma is available in standard or custom volumes. For documentation or international shipping, please contact learnmore@sanguinebio.com.

Applications

  • Immunology and translational research
  • Biomarker discovery and validation
  • Drug screening and assay development
  • Vaccine and infectious disease research

Product Features

  • Research Use Only (RUO), Bulk Plasma
  • Sourced from screened, consented donors
  • Processed under validated SOPs
  • QC tested for purity, viability, and sterility
  • Processed within 24 hours of collection
  • IRB-approved protocols with electronic informed consent

Donor Metadata

  • Verified diagnosis and clinical history
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Medication and treatment background when available

Compliance and Quality Assurance

  • IRB-approved collections and standardized procedures
  • 21 CFR Part 11-compliant e-consent system
  • HIPAA-compliant data management

Ordering & Customization

Human Bulk Plasma are available in customizable aliquot sizes. For international orders or documentation needs, please contact learnmore@sanguinebio.com to confirm requirements and availability. We also work with multiple ordering platforms and distributors, learn more here.

Where can I find your complete catalog?
How long can samples be stored?

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

What customization options are available?

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

Do you offer prospective collections?

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.

What is the turnaround time for custom collections?

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

Do you have samples in stock?

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

What does unique donor mean?

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

Are samples collected under IRB-approved protocols?

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 Bulk Plasma cohort?

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

More Information