Acute Myeloid Leukemia Plasma

In Stock Samples

Lot Number Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
75968 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 61 Female 18 $667.00
75966 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 78 Male 18 $667.00
75965 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 75 Female 24 $667.00
75968 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 61 Female 1 $667.00
75964 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 71 Female 23 $667.00
75964 Acute Myeloid Leukemia (AML) 1.0 ML Hispanic/Latino 71 Female 2 $667.00

Acute Myeloid Leukemia Plasma | High-Quality Human Plasma from Acute Myeloid Leukemia (AML) Donors

Acute Myeloid Leukemia Plasma is collected from donors clinically diagnosed with acute myeloid leukemia (AML) and processed within hours of collection to preserve key analytes such as cytokines, proteins, and metabolites. This human AML plasma supports research focused on biomarker discovery and monitoring, and treatment development for AML.

Product Features

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

De-identified Donor Data

  • Verified AML diagnosis
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Additional AML-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

Acute Myeloid Leukemia 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

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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 – with the exception of GMP leukopaks, all our products are research use only (RUO).

Our complete catalog can be found here: https://sanguinebio.com/products/

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 colleciton services to tailored to fit your research. For more information and request a quote, please see: https://sanguinebio.com/prospective-biospecimen-collection-services/

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 which can be found here https://sanguinebio.com/products/?pro_inventory=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: https://sanguinebio.com/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 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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