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, 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.
Leukopaks are collected by leukapheresis and typically provide high cell viability and functional immune cell populations at release, suitable for downstream research and manufacturing applications. Fresh leukopaks generally show excellent immediate viability and preserved functionality of T cells, B cells, NK cells, and monocytes, while cryopreserved leukopaks are processed using controlled‑rate freezing to maintain robust post‑thaw viability and functional recovery. Actual viability and functional performance may vary depending on donor characteristics, processing, storage, and the specific assay or application used.
All biospecimens are collected under Ethics Committee/IRB‑approved protocols with informed consent, and are handled in alignment with GCP, GLP, and GDPR requirements.
We support donor recall by operating two plasma donation centers (Heidelberg and Munich, Germany) and performing leukopak collections routinely, enabling reliable access to repeat donations. With donor consent and eligibility confirmed for each visit, pre‑screened donors can be re‑contacted and scheduled for follow‑up collections to support longitudinal studies or consistent manufacturing inputs. Recall timing and availability depend on donor eligibility, health status at the time of collection, and scheduling capacity.
Leukopaks are available in quarter, half, full, and double formats, corresponding to approximately ≥2.5, ≥5, ≥10, and ≥20 billion total cells, respectively. Customers can select from a range of additional QC and characterization options, including extended immunophenotyping by flow cytometry, HLA typing, and other custom assays. Custom donor inclusion or exclusion criteria can be applied based on clinical, demographic, or immunological requirements. In addition, logistics and delivery solutions can be tailored to match your required timelines, whether for time‑critical fresh deliveries or flexible cryopreserved supply.
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