Crohn’s Disease Serum
About:Crohn's Disease Serum from consented donors with clinically confirmed Crohn's disease, processed and frozen within 24 hours of collection. Serum is the conventional matrix for IBD serology such as ASCA and pANCA, for TNF and IL-23/Th17 cytokine panels, and for biologic trough and anti-drug antibody assays. Donors can be stratified by disease activity, Montreal location and behaviour, and treatment status, with matched healthy controls available.
About Crohn’s Disease Serum
Crohn’s Disease Serum for Immune-Mediated Inflammatory Bowel Disease Research
Our Crohn’s Disease Serum is sourced from IRB-consented donors clinically diagnosed with Crohn’s disease. Each sample is processed and frozen within 24 hours of collection to ensure consistency and high quality for inflammation and immunology studies. Crohn’s disease is an immune-mediated inflammatory bowel disease driven by a dysregulated mucosal response to the gut microbiota in genetically susceptible individuals, not by a classical autoantibody response.
Why Serum for Crohn’s Disease Research
- Serum is the conventional matrix for the antibody assays used in IBD serology, including anti-Saccharomyces cerevisiae antibodies (ASCA), anti-OmpC and pANCA. ASCA are antibodies to a microbial antigen rather than autoantibodies, and the ASCA-positive/pANCA-negative pattern is used to help differentiate Crohn’s disease from ulcerative colitis.
- Serum removes fibrinogen and most clotting factors, giving a lower-viscosity, lower-interference matrix for many commercial ELISA and multiplex immunoassay kits validated on serum.
- Crohn’s inflammation is driven by the IL-12/IL-23, Th1/Th17 and TNF axis. Serum supports quantification of the circulating mediators of that axis, including TNF, IL-6, IL-17A and IL-22, alongside acute-phase CRP.
- Biologic trough concentrations and anti-drug antibodies against anti-TNF, anti-IL-23 and anti-integrin therapies are routinely measured in serum, making it the practical matrix for therapeutic drug monitoring assay development.
- Serum from stricturing disease supports research on extracellular matrix turnover and fibrosis markers, which reflect the transmural remodelling that distinguishes Crohn’s disease from mucosa-limited colitis.
- Because clotting activates platelets and complement, serum and plasma are not interchangeable for those analytes; ordering matched serum and plasma from the same donors lets teams anchor cross-matrix comparability.
Donor Stratification Available
- Disease activity, including clinical remission versus active flare, with Harvey-Bradshaw Index or CDAI where documented
- Montreal classification: age at diagnosis, disease location (ileal, colonic, ileocolonic, upper GI) and behaviour (non-stricturing, stricturing, penetrating)
- Serology and laboratory results where available, including ASCA status, CRP and faecal calprotectin
- Treatment status: biologic-naive, anti-TNF, anti-IL-12/23 or anti-IL-23, anti-integrin, JAK inhibitor, corticosteroid or immunomodulator
- Surgical and complication history, including prior resection, ostomy and perianal fistulising disease
- Matched healthy controls available, as well as ulcerative colitis donors for IBD subtype comparison
Product Features
- Collected from clinically confirmed Crohn’s disease donors
- Research Use Only (RUO)
- Processed and frozen within 24 hours of collection
- IRB-approved protocols with documented consent
- Standard and custom aliquot volumes; volumes reported per lot
- Matched plasma and whole blood from the same donors available on request
De-identified Donor Data
- Diagnosis confirmation
- Age, sex assigned at birth, and ethnicity
- Donor-reported allergy and infectious disease history
- Medication history and Crohn’s disease-specific metadata available on request
Applications
- ASCA, anti-OmpC and pANCA serology assay development and IBD subtype discrimination
- Serum cytokine and inflammatory protein profiling across the TNF and IL-23/Th17 axes
- Biomarker discovery and validation for disease activity and mucosal healing
- Therapeutic drug monitoring and anti-drug antibody assay development
- Fibrosis and extracellular matrix turnover marker research in stricturing disease
- Serum proteomics and metabolomics
- Therapeutic candidate screening and target validation
- Disease-state control matrix for immunoassay qualification and kit validation
Other Crohn’s Disease Specimen Types
- Crohn’s Disease Plasma
- Crohn’s Disease Whole Blood
- Crohn’s Disease PBMC
- Crohn’s Disease Leukopak
- Crohn’s Disease Bulk Plasma
- Crohn’s Disease CD19+ B Cells
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
Crohn’s disease serum is available in standard and custom volumes. For pricing, current availability, or a quote on a stratified donor cohort, email learnmore@sanguinebio.com. For international orders or documentation requirements, please contact us to ensure compatibility with your country’s regulations. To browse other disease states in this specimen type, visit our human serum page.
Applications
- Immunology and translational research
- Biomarker discovery and validation
- Drug screening and assay development
- Vaccine and infectious disease research
Product Features
- Research Use Only (RUO), Serum
- Sourced from screened, consented donors
- Processed under validated SOPs
- QC tested for purity, viability, and sterility
- Processed within 24 hours of collection
- IRB-approved protocols with electronic informed consent
Donor Metadata
- Verified diagnosis and clinical history
- Demographic data: age, sex assigned at birth, race/ethnicity
- Medication and treatment background when available
Compliance and Quality Assurance
- IRB-approved collections and standardized procedures
- 21 CFR Part 11-compliant e-consent system
- HIPAA-compliant data management
Ordering & Customization
Human Serum are available in customizable aliquot sizes. For international orders or documentation needs, please contact learnmore@sanguinebio.com to confirm requirements and availability. We also work with multiple ordering platforms and distributors, learn more here.
Protocols & Documentation
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Download
Serum Isolation
Protocol for serum preparation from whole blood, including collection handling, clarification, and quality documentation.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Serum
Where can I find your complete catalog?
You can find our full product catalog here.
How long can samples be stored?
Storage depends on sample type but often cryopreserved samples stored in liquid nitrogen can be stored for years.
What customization options are available?
Extensive customization is available. To discuss your project request a quote or email us at learnmore@sanguinebio.com.
Do you offer prospective collections?
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.
What is the turnaround time for custom collections?
Timelines depend on condition, sample type, and I/E criteria but we often start collection within 2 weeks of signed agreement.
Do you have samples in stock?
YES - we have in-stock inventory. You can also email us at learnmore@sanguinebio.com as we continually get new samples in our inventory.
What does unique donor mean?
Each sample from a different individual - Unique donor means each sample comes from a different person, ensuring biological diversity in your study.
Are samples collected under IRB-approved protocols?
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.
Frequently Asked Questions
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100 In Stock View InventoryNeed a custom Serum cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.