Leukopaks

Access high-quality leukopaks:

  • 24h delivery of fresh samples accross Central Europe
  • Next day delivery of cryopreserved leukopaks
    (in stock/stored at -150°C liquid nitrogen)
  • Large, recallable donor pool
  • Weekly collection scheduling
  • Detailed clinical data incl. complete donor demographics, ICD-code & treatment status/medication 
  • IRB/EC-approved & fully consented sample collection in Germany

Request high-quality Leukopaks

Submit a request to inquire about Leukopaks.

The request should include key project details, such as:

  • Donor health/disease status
  • Fresh or cryopreserved formats
  • Size (≥2.5 to ≥20 billion total cells
  • Additional information (e.g. Donor, QC or processing requirements)

Get in contact and schedule a meeting with our team to discuss the next steps.

Cell number/bag size: ≥ 2.5 × 10⁹ to ≥20 × 10⁹ mononuclear cells per bag.

Collection & processing: Leukapheresis using the Spectra Optia™ apheresis system. Cryopreserved leukopaks are processed on the day of collection. 

Hematology analysis: Quantification of total leukocytes, erythrocytes, platelets, differential white blood cell populations (neutrophils, lymphocytes, monocytes) is performed using a Sysmex XN‑330.

Anticoagulant: Acid-citrate-dextrose solution A (ACD-A).

Additional characterization: viability, HLA-typing, FACS analysis, HLH analysis, mycoplasma testing and additional laboratory parameters available upon request.

Storage & shipping: Fresh leukopaks stored at 2–8 °C after collection and cryopreserved leukopaks at -150 °C in LN₂; shipped on dry ice or dry shipper within 24 hours in Central Europe.

Donor demographics: Age, gender, weight, height, BMI, ethnicity, smoking and alcohol consumption status, country of collection, and collection date and time.

Serology: Serological testing for Anti-HIV, Anti-HCV and HBsAg is performed in-house using CE-approved assays.

Immunogenetics: 6-digit resolution HLA Class I and Class II characterization (on demand).

Clinical background: Disease, medication, allergies (self-reported). Customization options to individual requirements.

All data are provided in accordance with ethical approvals, informed consent, and applicable data protection regulations.

The publications below illustrate the application of our products in research settings.

  • Ogusuku, I.E.Y.; Herbel, V.; Lennartz, S.; Brandes, C.; Argiro, E.; Fabian, C.; Hauck, C.; Hoogstraten, C.; Veld, S.; Hageman, L.; et al. Automated Manufacture of ΔNPM1 TCR-Engineered T Cells for AML Therapy. Molecular Therapy – Methods & Clinical Development 2024, 32, 101224.

    https://doi.org/10.1016/j.omtm.2024.101224 


 

 

Questions? We’ve got answers

What compliance and ethics standards apply to our samples?

All samples are either anonymized left-over material from standard-of-care/routine diagnostics or have been prospectively collected or are part of a plasma donation. We confirm, that all samples have been obtained in compliance with the applicable legal and ethical requirements prevailing in the country of origin. The samples provided by us could be used for research and/or development and/or validation purposes. 

How can I partner with BIOMEX for my project?

Your success is our focus. Learn more about how we work.

How can I purchase from BIOMEX?

Choose the option that works best for you:

Visit our website
Explore our services, capabilities, and available biospecimens.

Browse in the Sample Shop
Register for full access and request directly online.

Submit a request form
Send us the details of what you need — we’ll respond promptly.

Or contact us directly by email or phone.
р +49 6221 4166-0
e sales at biomex.de

How do I contact customer support?

Simply contact our German office:

р +49 6221 4166-0
e sales at biomex.de

Empowering scientists with trusted starting materials

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Worldwide shipping

Based in Heidelberg, Germany, BIOMEX ships biospecimens worldwide using compliant, temperature‑controlled logistics.

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Certified quality

BIOMEX operates an ISO 9001:2015–certified quality management system, audited regularly to ensure compliance and operational excellence.

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Ethically compliant

All biospecimen collections follow GCP, GLP, and GDPR requirements, with full Ethics Committee / IRB approval.