Multiple Myeloma PBMC

In Stock Samples

Lot # Condition Cell Count (M) Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
77844 Multiple Myeloma 10M Hispanic/Latino 80 Female 6
78676 Multiple Myeloma 10M 61 Male Ukraine
No medications
1
78677 Multiple Myeloma 10M 61 Male Ukraine
No medications
1
78678 Multiple Myeloma 10M 61 Male Ukraine
No medications
1
78588 Multiple Myeloma 10M 65 Female Ukraine
Perindopril, Bortezomib, Lenalidomide, Dexamethasone
1
78707 Multiple Myeloma 10M 53 Male Ukraine
Enalapril, Bortezomib, Cyclophosphamide, Dexamethasone
1
78589 Multiple Myeloma 10M 65 Female Ukraine
Perindopril, Bortezomib, Lenalidomide, Dexamethasone
1
78691 Multiple Myeloma 10M 61 Female Ukraine
Amlodipine, Cyclophosphamide, Mesna, Bortezomib
1
78657 Multiple Myeloma 10M 58 Male Ukraine
No medications, Cyclophosphamide, Lomustine, Melphalan
1
78590 Multiple Myeloma 10M 65 Female Ukraine
Perindopril, Bortezomib, Lenalidomide, Dexamethasone
1

Multiple Myeloma PBMC for Tumour Immunology Research

Human Multiple Myeloma PBMC products are sourced from IRB-consented donors clinically diagnosed with multiple myeloma, processed within 24 hours of collection and cryopreserved in CryoStor® CS10 to preserve viability and function. These peripheral blood mononuclear cells enable study of immune evasion, effector-cell dysfunction and treatment resistance in a plasma-cell malignancy, and are available in cell counts from 5 million to 2 billion.

Why Multiple Myeloma PBMC for Tumour Immunology Research

Multiple myeloma is a neoplastic disorder of terminally differentiated plasma cells. Clonal plasma cells accumulate in the bone marrow and secrete a monoclonal immunoglobulin or free light chain, producing bone disease, renal impairment, anaemia and hypercalcaemia. It is a cancer, not an autoimmune disease, and its immunology is that of a tumour that both suppresses and is targeted by the host immune system.

  • Plasma-cell lineage antigens — CD38, BCMA, SLAMF7 and GPRC5D define the malignant compartment and are the antigens behind the current wave of antibody, bispecific and CAR-T therapeutics.
  • T-cell dysfunction and exhaustion — repeated antigen exposure and a suppressive marrow microenvironment drive inhibitory receptor expression and reduced effector capacity, which can be characterised directly in donor PBMCs.
  • Immunosuppressive cell populations — regulatory T cells and myeloid-derived suppressor cells expand in myeloma and blunt anti-tumour responses.
  • NK cell effector function — NK cells mediate antibody-dependent cellular cytotoxicity, the mechanism underlying anti-CD38 antibody therapy, and their function in disease-state donors differs from that of healthy cells.
  • Circulating plasma cells and clonal detection — a subset of donors carries measurable circulating clonal plasma cells, supporting minimal-residual-disease and clonality workflows on peripheral blood.
  • Cellular specimen advantage — because PBMCs are viable nucleated cells, flow cytometry, cytotoxicity assays, redirected-killing potency assays, single-cell transcriptomics and TCR repertoire work are all available; none of these are possible in a plasma or serum product.

Donor Stratification Available

  • Disease phase — newly diagnosed, on-treatment, in remission, and relapsed or refractory donors
  • Monoclonal protein class — IgG, IgA and light-chain-only disease, subject to documentation
  • Precursor and related conditions — MGUS and smouldering myeloma donors as comparators where available
  • Treatment exposure — proteasome inhibitor, immunomodulatory drug, anti-CD38 antibody, and post-autologous-transplant donors
  • Cytogenetic risk category and demographics — where documented, plus age, sex assigned at birth and race/ethnicity
  • Matched healthy controls available, drawn on the same protocol and matched for age, sex and ethnicity

Product Features

  • Research Use Only (RUO), cryopreserved PBMCs
  • Clinically confirmed multiple myeloma donors
  • Available in cell counts ranging from 5 million to 2 billion
  • Processed within 24 hours of collection
  • Stored using CryoStor® CS10 freezing media
  • IRB-approved protocols and electronic informed consent
  • Screen LeukoLot™ available prior to bulk orders

De-identified Donor Data

  • Verified multiple myeloma diagnosis
  • Donor demographics: age, sex assigned at birth, race/ethnicity
  • Self-reported allergies and infectious disease history
  • Disease phase and prior treatment context reported per lot where captured
  • Additional multiple myeloma-specific data available upon request

Applications

  • BCMA, GPRC5D and SLAMF7-directed bispecific and CAR-T potency assays
  • Anti-CD38 antibody-dependent cellular cytotoxicity and NK effector function studies
  • T-cell exhaustion and effector dysfunction immunophenotyping
  • Regulatory T cell and myeloid-derived suppressor cell characterisation
  • Autologous effector-cell sourcing for redirected-killing assay development
  • Circulating clonal plasma cell detection and minimal-residual-disease workflow development
  • Single-cell transcriptomic and proteomic profiling of the myeloma immune compartment
  • Drug screening, resistance modelling and biomarker discovery in myeloma pathophysiology

Other Multiple Myeloma Specimen Types

Compliance and Quality Assurance

  • IRB-approved collections and protocols
  • 21 CFR Part 11-compliant e-consent system
  • HIPAA-compliant donor data protection

Ordering & Customization

Multiple Myeloma PBMC samples are shipped on dry ice and available in custom aliquots. For pricing, international orders or regulatory requirements, please contact learnmore@sanguinebio.com to confirm documentation and compliance needs. To compare collection formats or check wider availability, visit our human PBMCs page.

Protocols & Documentation

  • PBMC Isolation from Whole Blood

    Standard operating procedure for isolating peripheral blood mononuclear cells from whole blood using density-gradient separation.

    Download
  • Immune Cell Isolation

    Guidelines for isolating immune cell populations with validated enrichment steps, purity checkpoints, and documentation.

    Download
  • Choosing the Right PBMC Configuration

    Reference guide comparing PBMC formats, cryopreservation states, and study-fit recommendations for your application.

    Download
  • Thawing Cryopreserved PBMC

    Validated thawing protocol to recover viable cryopreserved PBMCs while minimizing activation and loss of function.

    Download
  • Informed Consent Form (ICF)

    Available upon request — confirms donor consent for research use and downstream commercialization.

PBMC

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 PBMC 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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