Pemphigoid Leukopak
About: LeukoCore Pemphigoid Leukopak products contain concentrated immune cells from donors with clinically confirmed pemphigoid, collected via apheresis. Ideal for high-yield studies on autoantibody-mediated skin diseases, immune dysregulation, and biomarker discovery in subepidermal blistering disorders.
LeukoCore Pemphigoid Leukopak for Immunology Research
LeukoCore Pemphigoid Leukopak biospecimens are collected from donors clinically diagnosed with Pemphigoid through IRB-approved apheresis procedures. Each leukopak contains large quantities of peripheral blood mononuclear cells (PBMCs), making it ideal for immune profiling, cytokine analysis, and drug development research related to Pemphigoid-associated inflammation and immune dysregulation.
Product Features
- Research Use Only (RUO) human leukopaks
- Clinically confirmed Pemphigoid donors
- High cell yield for large-scale studies
- Processed and shipped within 24 hours of collection
- Fresh or cryopreserved options available
- IRB-approved and ethically sourced
- Infectious disease testing
- HLA-A typing
- Screen donors with LeukoLot™
De-identified Donor Data
- Verified Pemphigoid diagnosis from healthcare providers
- Donor demographics: age, sex assigned at birth, race/ethnicity
- Self-reported medication history and allergies
- Relevant clinical data Pemphigoid
Applications
- Immune cell characterization in Pemphigoid
- Therapeutic development and screening
- Cell-based assays and cytokine profiling
- Multi-omics studies single-cell sequencing
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
Pemphigoid Leukopak samples are available fresh or cryopreserved. For international shipping or regulatory documentation, please contact learnmore@sanguinebio.com to confirm regional compliance and shipping availability.
Protocols & Documentation
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Leukopak Cryopreservation
Standard operating procedure for cryopreserving leukopak units with controlled freezing and post-thaw viability targets.
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Leukopak Thawing
Validated thawing workflow for cryopreserved leukopaks to maximize recovery while maintaining sterility and chain of custody.
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Choosing the Right PBMC Configuration
Reference guide comparing PBMC formats, cryopreservation states, and study-fit recommendations for your application.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Leukopak
Frequently Asked Questions
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All our samples have self-reported infectious disease testing and verified clinical diagnosis. Many of our samples have the option of electronic medical records provided and our prospective collection offers the opportunity for patient reported outcomes and surveys. Learn more here. https://sanguinebio.com/patient-reported-outcomes-pro-surveys-questionnaires/
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YES – Certificate of analysis is available upon request.
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Lead times vary from ready to ship inventory to prospective studies.
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International shipping is available. We also work with a number of distributors. Contact us to discuss options at learnmore@sanguinebio.com.
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We have several ordering methods. You can order directly online with a PO or credit card or contact us to have a sales specialist help with your order. https://sanguinebio.com/request-quote/
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You can request a quote on this page or contact us at learnmore@sanguinebio.com. https://sanguinebio.com/request-quote/
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NO – no minimum order requirements.
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For bulk pricing inquiries, please contact: LearnMore@sanguinebio.com
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YES – Unique donors can be specified.
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International shipping is available. For more information and documentation requirements, please contact learnmore@sanguinebio.com.
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YES – We offer cryopreservation of leukopaks and PBMC processing, aliquoting, and cryopreservation.
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YES – We offer full and half size leukopaks both fresh and cryopreserved.
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.