Type 1 Diabetes Leukopak

In Stock Samples

Lot # Condition Bag Size Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
56980 Diabetes Type I Asian/Pacific Islander 34 Male United States
GLARGINE 24 UNITS/24 LANTIS INSULIN 8UNITS/18UNITS/15UNITS MILD DIABETIC RETINOPATHY
1
55922 Diabetes Type I Half Bag Hispanic/Latino 46 Male United States
Atorvastatin 40mg qd, Losartan 50mg qd, Pantoprazole 20mg bid, Humalog with Insulin pump
1 $10,500.00
59332 Diabetes Type I Full Bag Hispanic/Latino 34 Male United States
Himalogue pump - based on 1 for every 7 carts None
1 $15,225.00
57651 Diabetes Type I Half Bag Caucasian 36 Female United States
Humalog/40units / QD, TRESIBA 16 U IN MORN/10 AT NIGHT
1 $10,500.00
59332 Diabetes Type I Full Bag Hispanic/Latino 34 Male United States
Himalogue pump - based on 1 for every 7 carts None
3 $15,225.00

High-Yield LeukoCore Type 1 Diabetes Leukopak for Autoimmune Immunology Research

LeukoCore Type 1 Diabetes Leukopak biospecimens are collected from IRB-consented donors clinically diagnosed with type 1 diabetes (T1D) through IRB-approved apheresis procedures. Each leukopak contains large quantities of peripheral blood mononuclear cells (PBMCs), making it suited to studies that require high input cell numbers.

Why a Leukopak for Type 1 Diabetes Research

T1D is a T cell–mediated autoimmune disease in which cytotoxic lymphocytes destroy insulin-producing pancreatic beta cells. The central experimental problem is that the cells responsible are extremely rare in circulation, and a standard blood draw simply does not contain enough of them. A leukopak solves the numbers problem.

  • Autoreactive T cells are rare — CD8 T cells recognising beta-cell antigens such as preproinsulin circulate at very low frequency, so tetramer or multimer-based detection and functional assays require the cell numbers only apheresis provides
  • Regulatory T cell isolation at scale — defective regulatory T cell control of autoreactive responses is a core feature of T1D, and Treg purification for phenotyping, suppression assays, or expansion feasibility work is yield-limited
  • HLA class II restriction shapes the response — T1D risk is strongly associated with HLA-DR and HLA-DQ haplotypes, and antigen-specific work depends on matching donor HLA type to the reagents used
  • Antigen-specific readouts need replicates — low-frequency responses require large-input, multi-replicate assay designs to achieve statistical confidence, which single-tube draws cannot support
  • Cell therapy and tolerance-induction feasibility — engineered regulatory T cell and antigen-specific tolerance approaches are assessed for manufacturing feasibility at scales only leukopaks reach
  • One donor, many assays — a single apheresis collection allows immunophenotyping, functional assays, and multi-omics on the same donor material, eliminating inter-donor variability as a confounder

Donor Stratification Available

  • Disease duration — new-onset within the first year versus long-standing disease
  • Islet autoantibody profile — GAD65, IA-2, ZnT8, and insulin autoantibody status where measured
  • Residual beta-cell function — C-peptide detectable versus undetectable where measured
  • HLA type — HLA-A typing included; extended class II typing available on request
  • Glycaemic control and treatment modality — HbA1c where recorded; injection, pump, or automated insulin delivery
  • Age at onset — paediatric versus adult onset; coexisting autoimmune disease where documented
  • Matched healthy controls available — demographically matched healthy donor leukopaks

Product Features

  • Research Use Only (RUO) human leukopaks
  • Clinically confirmed T1D donors
  • High cell yield for large-scale studies
  • Processed and shipped within 24 hours of collection
  • Fresh or cryopreserved options available
  • Cell yield and viability reported per lot
  • IRB-approved and ethically sourced
  • Infectious disease testing
  • HLA-A typing
  • Screen donors with LeukoLot™

De-identified Donor Data

  • Verified T1D diagnosis from healthcare providers
  • Donor demographics: age, sex assigned at birth, race/ethnicity
  • Self-reported medication history and allergies
  • Relevant clinical data including age at onset and disease duration (if available)

Applications

  • Antigen-specific autoreactive T cell detection by tetramer or multimer staining
  • Regulatory T cell isolation, phenotyping, and suppression assays
  • Immune cell characterisation and deep immunophenotyping in T1D
  • Cell-based assays, cytokine profiling, and functional readouts at scale
  • Multi-omics studies including single-cell and TCR repertoire sequencing
  • HLA-restricted antigen presentation research
  • Cell therapy and tolerance-induction feasibility studies
  • Therapeutic development, screening, and mechanism-of-action work

Other Type 1 Diabetes Specimen Types

Matched material from the same T1D donor pool is available as type 1 diabetes serum, plasma, whole blood, and PBMC. Isolated subsets are available as CD4+ T cells, CD8+ T cells, and CD19+ B cells.

Compliance and Quality Assurance

  • Collected under IRB oversight with donor e-consent (21 CFR Part 11 compliant)
  • HIPAA-compliant handling of donor information
  • Rigorous donor screening and documentation

Ordering & Customization

Type 1 Diabetes Leukopak samples are available fresh or cryopreserved. For pricing, or to check current availability across our full leukopak inventory, visit our human leukopak page to browse other disease-state options and live stock status. For international shipping or regulatory documentation, please contact learnmore@sanguinebio.com to confirm regional compliance and shipping availability.

Protocols & Documentation

  • Leukopak Cryopreservation

    Standard operating procedure for cryopreserving leukopak units with controlled freezing and post-thaw viability targets.

    Download
  • Leukopak Thawing

    Validated thawing workflow for cryopreserved leukopaks to maximize recovery while maintaining sterility and chain of custody.

    Download
  • Choosing the Right PBMC Configuration

    Reference guide comparing PBMC formats, cryopreservation states, and study-fit recommendations for your application.

    Download
  • Informed Consent Form (ICF)

    Available upon request — confirms donor consent for research use and downstream commercialization.

Leukopak

Frequently Asked Questions

Showing 1–12 of 24 results

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 – all our products are research use only (RUO).

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 collection services tailored to fit your research. For more information and to request a quote, please see: our prospective biospecimen collection services page.

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. 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: 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.

1
×

Ask a Question

Need a custom Leukopak cohort?

Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.

More Information