Flexible Leukopak supply
- Fresh or cryopreserved formats
- Sizes ranging from ≥2.5 to ≥20 billion total cells
- Healthy and selected disease‑state donors
- Recallable pre-screened donors
Blood Cells > Leukopaks

Fresh Leukopaks are collected in BIOMEX’s own plasma centers in Germany using the Spectra Optia™ apheresis system and acid‑citrate‑dextrose solution A (ACD‑A) as anticoagulant. Each leukopak delivers a high‑density mononuclear cell profile, typically enriched with up to 20% monocytes, 50% T cells, 10% B cells, and 10% natural killer cells, clearly outperforming buffy coat–derived material. Full documentation is included, such as donor metadata, HLA typing, complete blood count, and pathogen testing, with additional testing available on request.
Collection method: Leukapheresis using the Spectra Optia™ apheresis system
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)
Storage (fresh Leukopaks): Refrigerated temperature (2-8°C) directly after collection
Storage (cryo Leukopaks): Same‑day processing with controlled‑rate cryopreservation and storage in liquid nitrogen (vapor phase)
Donor demographics: Age, sex, race/ethnicity, BMI, smoking status
Serology: Anti-HIV 1/2, Anti-HCV, HBs-Ag
Immunogenetics: 6-digit resolution HLA Class I and Class II characterization (on demand)
Clinical background: Disease, medication, allergies (self-reported)
Ethics: All donor collections are conducted under informed consent and Institutional Review Board (IRB)–approved protocols
Depending on the requested donor and study requirements, additional donor information and sample characterization data can be provided on demand.
Based in Heidelberg, Germany, BIOMEX ships biospecimens worldwide using compliant, temperature‑controlled logistics.
BIOMEX operates an ISO 9001:2015–certified quality management system, audited regularly to ensure compliance and operational excellence.
All biospecimen collections follow GCP, GLP, and GDPR requirements, with full Ethics Committee / IRB approval.
Healthy donors are individuals who self‑report as being in good health based on a standardized donor questionnaire and eligibility assessment conducted prior to each collection. For every leukopak collection, donors undergo serological testing for key infectious diseases, including HIV, hepatitis B (HBV), and hepatitis C (HCV), to support product safety and quality. Only collections meeting these health and testing criteria are released as healthy donor leukopaks.
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