Multiple Myeloma Plasma

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
78631 Multiple Myeloma 1.0 ML 77 Female
Acetylsalicylic acid
1 $667.00
78712 Multiple Myeloma 1.0 ML 53 Male
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1 $667.00
78713 Multiple Myeloma 1.0 ML 53 Male
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1 $667.00
78632 Multiple Myeloma 1.0 ML 77 Female
Acetylsalicylic acid
1 $667.00
78714 Multiple Myeloma 1.0 ML 53 Male
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1 $667.00
78633 Multiple Myeloma 1.0 ML 77 Female
Acetylsalicylic acid
1 $667.00
78634 Multiple Myeloma 1.0 ML 77 Female
Acetylsalicylic acid
1 $667.00
78715 Multiple Myeloma 1.0 ML 53 Male
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1 $667.00
78716 Multiple Myeloma 1.0 ML 53 Male
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1 $667.00
78635 Multiple Myeloma 1.0 ML 77 Female
Acetylsalicylic acid
1 $667.00

Multiple Myeloma Plasma | High-Quality Human Plasma from Multiple Myeloma Donors

Multiple Myeloma Plasma is collected from donors clinically diagnosed with multiple myeloma and processed within hours of collection to preserve key analytes such as cytokines, proteins, and metabolites. This human plasma supports research focused on biomarker discovery in multiple myeloma pathophysiology.

Product Features

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

De-identified Donor Data

  • Verified multiple myeloma diagnosis
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Additional multiple myeloma-specific metadata available

Applications

  • Biomarker discovery and validation
  • Cytokine and inflammation profiling
  • Metabolomics and proteomics studies
  • Therapeutic response research

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

Multiple Myeloma 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.

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

Showing 25–31 of 31 results

Do plasma samples come with clinical information (autoantibody status, HbA1c values, IHC results, stage information, genetic mutation data)?

1 Answer

YES – Comprehensive medical records are available and may contain information regarding autoantibody status.

YES – Sanguine offers both inventory for select conditions, as well as, prospective collection. For inventory visit https://sanguinebio.com/products/plasma/?pro_inventory=inventory.

We never thaw our plasma samples before shipping.

Our standard aliquot size for plasma is 1 mL but we have bulk plasma (50 to 150 mL) available for select conditions. https://sanguinebio.com/product/human-bulk-plasma/

YES – Sanguine bio provides “age-matched healthy controls” and longitudinal studies capabilities.

YES – custom age specifications available – The “Specify I/E Criteria” service allows you to define specific age ranges for donor selection.

Age ranges available – Donor metadata includes age specifications, and you can specify inclusion/exclusion criteria. For pediatric samples specifically, contact learnmore@sanguinebio.com.

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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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