Crohn’s Disease Serum

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
71590 Crohn's Disease 1.0 ML Caucasian 25 Female United States
Skyrizi 180 mg Magnesium 100 ml spironolactone QD
2 $316.00
71039 Crohn's Disease 1.0 ML Caucasian 28 Female United States
Prozac 40 mg Lamictal 200 mg Gabapentin 300 mg Prazosin 5mg Inflectra infusion every 8 weeks- last infustion 8 weeks ago
4 $316.00
69974 Crohn's Disease 1.0 ML Caucasian 43 Male United States
Stelara 90 mg per ml allergy OTC meds Multi Vit
5 $316.00
69934 Crohn's Disease 1.0 ML Caucasian 32 Male United States 4 $316.00
69624 Crohn's Disease 1.0 ML Caucasian 28 Male United States
Prednisone no longer Humira 40mg every other week
4 $316.00
68907 Crohn's Disease 1.0 ML Caucasian 39 Male United States
Omeprazole 20mg 1x/day Liver pills Iron fish tea (lucky iron fish)
3 $316.00
68650 Crohn's Disease 1.0 ML Caucasian 45 Female United States
Mesalamine/Pentasa 500mg 8 times a day Venlafaxine 150mg QD Claritin 10mg QD Bupropion 75mg QD Quetiapine 25 MG QD
4 $316.00
67956 Crohn's Disease 1.0 ML Caucasian 50 Female United States
Humira 40 mg/1x week Omeprazole 40 mg/day Multivitamin b12 calcium probiotics
1 $316.00
67814 Crohn's Disease 1.0 ML Caucasian 25 Female United States
Skyrizi 180 mg Magnesium
4 $316.00
69938 Crohn's Disease 1.0 ML Caucasian 25 Female United States
Stelara 90 mg 1x every 4 weeks Testosterone Cypionate 80 mg 1x/week Lexipro 20 mg Abilfy 2mg Trileptal 600 mg Omeprazole 40 mg Buspra 10 mg 3x/day Azithromycin 40 mg 3x/day- Prescribed on 2025 -no longer taking Amitriptyline 20 mg/day
5 $316.00

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

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.

Protocols & Documentation

  • Serum Isolation

    Protocol for serum preparation from whole blood, including collection handling, clarification, and quality documentation.

    Download
  • Informed Consent Form (ICF)

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

Serum

Frequently Asked Questions

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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.

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Need a custom Serum cohort?

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

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