Hidradenitis Suppurativa Plasma
Hidradenitis Suppurativa Plasma from IRB-consented donors with clinically confirmed HS, a chronic immune-mediated inflammatory skin disease of follicular occlusion. Ideal for identifying circulating inflammatory cytokines and severity-correlated biomarkers, and for TNF and IL-17 pathway research. Hurley stage stratification available.
| Lot # | Condition | Volume | Race/Ethnicity | Age | Gender | Country of Collection | Medications | Vials | Price | Action |
|---|---|---|---|---|---|---|---|---|---|---|
| 74920 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | 30 | Male |
Ketoconazol champu
|
13 | $495.00 | ||
| 74921 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | 61 | Male |
Ozempic 2mg SC Meekly, Basaglar 30u SCQD, MEtformin 1000mg POQD, Atorvastatin 20mg POQD, /jardiance
|
12 | $495.00 | ||
| 74919 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | -1 | Female |
Enalapril Hidroclorotiazida
|
19 | $495.00 | ||
| 70586 | Hidradenitis Suppurativa | 5.0 ML | Caucasian | 46 | Female | United States |
Citroline 250mg QD Simotriptin as needed
|
1 | $495.00 | |
| 49182 | Hidradenitis Suppurativa | 2.0 ML | Hispanic/Latino | 30 | Female | United States |
GABBAPENTIN 300MG, QD birth control Lamotrigine 200mg QD Adderall 15mg QD
|
13 | $495.00 | |
| 53604 | Hidradenitis Suppurativa | 2.0 ML | Hispanic/Latino | 41 | Female | United States | 5 | $495.00 | ||
| 74921 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | 61 | Male |
Ozempic 2mg SC Meekly, Basaglar 30u SCQD, MEtformin 1000mg POQD, Atorvastatin 20mg POQD, /jardiance
|
8 | $495.00 | ||
| 74920 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | 30 | Male |
Ketoconazol champu
|
12 | $495.00 | ||
| 77115 | Hidradenitis Suppurativa | 1.0 ML | African American | 37 | Female | 7 | $495.00 | |||
| 74919 | Hidradenitis Suppurativa | 1.0 ML | Hispanic/Latino | -1 | Female |
Enalapril Hidroclorotiazida
|
6 | $495.00 |
Hidradenitis Suppurativa Plasma for Immune-Mediated Inflammatory Disease Research
Hidradenitis Suppurativa Plasma is collected from IRB-consented donors clinically diagnosed with hidradenitis suppurativa (HS) and processed within one day of collection to preserve key analytes such as cytokines, proteins and metabolites. HS is a chronic immune-mediated inflammatory skin disease of the hair follicle and adjacent apocrine gland-bearing skin, in which follicular occlusion and rupture trigger a deep, destructive inflammatory response producing painful nodules, abscesses, draining tunnels and scarring. This human plasma supports inflammatory pathway research and biomarker discovery.
Follicular Occlusion, Innate Inflammation and Why Plasma
- The initiating event is follicular occlusion and rupture, which releases follicular contents into the dermis and provokes an intense neutrophil- and macrophage-rich inflammatory response. HS is immune-mediated and inflammatory, not autoimmune.
- Lesional and circulating cytokine profiles implicate TNF-alpha, IL-17 and IL-1 family signalling, which is the rationale for the TNF and IL-17 pathway biologics now used in HS.
- HS carries a substantial systemic inflammatory burden, with elevated acute-phase reactants including CRP frequently observed and correlating with disease severity.
- Secondary bacterial colonisation and biofilm formation within tunnels contribute to the inflammatory cycle without HS being a primary infectious disease.
- HS is strongly associated with metabolic comorbidity, including obesity and metabolic syndrome, and with other immune-mediated conditions such as inflammatory bowel disease — making plasma a useful matrix for studying shared systemic inflammation.
- Plasma is acellular. It supports cytokine and acute-phase protein immunoassay, proteomic and metabolomic profiling, but not flow cytometry or other cell-based assays.
Donor Stratification Available
- Hurley stage I, II or III as documented
- Anatomical distribution and number of affected sites where documented
- Treatment status: topical or oral antibiotics, TNF or IL-17 pathway biologic, retinoid, or treatment-naive
- Presence of metabolic comorbidity, including obesity, metabolic syndrome or type 2 diabetes
- Associated immune-mediated comorbidity such as inflammatory bowel disease or spondyloarthritis
- Smoking status where documented
- Matched healthy controls available
Product Features
- Research Use Only (RUO)
- Plasma collected from clinically confirmed HS donors
- Processed within one day of collection
- Anticoagulant selection available on request
- IRB-approved protocols and informed consent
- Custom aliquot volumes available upon request
De-identified Donor Data
- Verified HS diagnosis, with Hurley stage where documented
- Demographic data: age, sex assigned at birth, race/ethnicity
- Donor-reported medications, allergies, and comorbidities
- Additional hidradenitis suppurativa-specific metadata available
Applications
- TNF-alpha, IL-17 and IL-1 family cytokine profiling
- Acute-phase reactant and systemic inflammatory burden characterisation
- Severity-correlated biomarker discovery and validation
- Biologic therapy response and pharmacodynamic biomarker research
- Plasma proteomic and metabolomic discovery studies
- Neutrophil-associated mediator and protease profiling
- Shared-pathway research across immune-mediated inflammatory diseases
- Metabolic comorbidity and systemic inflammation crossover studies
Other Hidradenitis Suppurativa Specimen Types
- Hidradenitis Suppurativa Bulk Plasma
- Hidradenitis Suppurativa Serum
- Hidradenitis Suppurativa Whole Blood
- Hidradenitis Suppurativa PBMC
- Hidradenitis Suppurativa Leukopak
- Hidradenitis Suppurativa Skin Punch Biopsy
Compliance and Quality Assurance
- IRB-approved and HIPAA-compliant protocols
- Electronic informed consent with 21 CFR Part 11 – compliant e-signatures
- Documentation support available for regulatory review
Ordering & Customization
Hidradenitis suppurativa plasma is available in standard and custom volumes. For pricing, current availability, international orders or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations. To browse donor cohorts across our full inventory, visit our human plasma page.
Protocols & Documentation
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Download
Plasma Isolation
Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Plasma
Frequently Asked Questions
1 Answer
YES – All collections are conducted under IRB-approved protocols and electronic informed consent. Sanguine utilizes Advarra and WCG IRB for oversight.
1 Answer
YES – all our products are research use only (RUO).
1 Answer
You can find our full product catalog here.
1 Answer
Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.
1 Answer
Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.
1 Answer
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.
1 Answer
Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.
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YES – we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.
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Each sample from a different individual – Unique donor means each sample comes from a different person, ensuring biological diversity in your study.
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YES – Unique donors can be specified and guaranteed based on your requirements.
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For information about sample quality, please see: Quality and Compliance
1 Answer
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.
Ask a Question
Need a custom Plasma cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.