Acute Myeloid Leukemia (AML) Bone Marrow Mononuclear Cells
Acute Myeloid Leukemia (AML) Bone Marrow Mononuclear Cells - cryopreserved BMMCs isolated from clinically confirmed AML donors. AML is diagnosed and staged by marrow myeloblast percentage, making marrow the essential specimen for diagnosis, risk stratification, and MRD monitoring. Ideal for FLT3/NPM1 molecular studies, blast immunophenotyping, and targeted therapy research. Stratification by cytogenetic/molecular risk group and treatment phase.
Acute Myeloid Leukemia (AML) Bone Marrow Mononuclear Cells for Leukemia Research
Our Acute Myeloid Leukemia (AML) Bone Marrow Mononuclear Cells is a hematopoietic tissue sample isolated by density-gradient separation from bone marrow aspirate, capturing the full spectrum of marrow-resident hematopoietic stem, progenitor, and precursor cells that peripheral blood samples do not contain. Samples are sourced from IRB-consented donors clinically diagnosed with AML, an aggressive myeloid malignancy defined by marrow blast accumulation.
AML Biology and Why Bone Marrow
- AML diagnosis requires a marrow myeloblast count of 20% or greater (per WHO criteria), making bone marrow aspirate the required diagnostic specimen rather than peripheral blood, which may not reflect true marrow blast burden.
- Cytogenetic and molecular risk stratification – including FLT3-ITD, NPM1, CEBPA, and TP53 status – is performed on marrow aspirate and directly informs treatment intensity and eligibility for targeted therapies.
- Minimal residual disease (MRD) assessment by flow cytometry or molecular methods on post-treatment marrow is a key determinant of relapse risk and consolidation strategy.
- Targeted agents including FLT3 inhibitors, IDH1/2 inhibitors, and venetoclax-based regimens have made marrow-derived blast material essential for pharmacodynamic and resistance-mechanism studies.
- Marrow stromal and microenvironment interactions are an active area of research into AML chemoresistance and relapse.
Donor Stratification Available
- Cytogenetic and molecular risk group (favorable, intermediate, adverse)
- Key mutation status where documented: FLT3, NPM1, CEBPA, TP53, IDH1/2
- Disease phase: newly diagnosed, post-induction, relapsed/refractory
- Blast percentage at collection where available
- Treatment history, including targeted agents or stem cell transplant
- Age band and sex assigned at birth
- Matched healthy bone marrow controls available
Product Features
- Isolated from clinically confirmed AML donor bone marrow aspirate
- Density-gradient purified and cryopreserved
- Research Use Only (RUO)
- IRB-approved protocols with documented consent
- Standard and custom cell quantities available
De-identified Donor Data
- AML diagnosis confirmation and cytogenetic/molecular subtype where documented
- Age, sex assigned at birth, and ethnicity
- Donor-reported allergy and infectious disease history
- Treatment history and disease phase where documented
- Additional AML-specific metadata available on request
Applications
- Minimal residual disease (MRD) detection and monitoring assay development
- FLT3, NPM1, and other molecular marker studies
- Targeted therapy pharmacodynamic and resistance-mechanism research
- Blast immunophenotyping studies
- Marrow microenvironment and chemoresistance research
Other Specimen Types
For matched marrow-derived material across conditions, see our human bone marrow mononuclear cells collection.
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 & Customization
AML bone marrow mononuclear cells are available in standard and custom cell quantities. For pricing, international orders, or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations.
Protocols & Documentation
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Frequently Asked Questions
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Need a custom Bone Marrow Mononuclear Cells cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.