Psoriasis Serum

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
77429 Psoriasis 1.0 ML Hispanic/Latino 49 Female United States
Skyrizi 150mg (injection) every 3 months
4 $316.00
75687 Psoriasis 1.0 ML Caucasian 21 Male United States
54 mg Methylphenidate (brand name Concerta), once per day in the morning. For ADHD. 5 mg guanfacine (brand name Tenex). Twice per day. Once in the morning, once at night. For ADHD. 100 mg + 250 mg (250 mg) fluvoxamine (brand name Luvox) at night. For OCD. 25 mg metorprolol, once per day at night. For tachycardia. 40 mg atomoxetine (brand name Strattera) once per day at night. For ADHD. 5 mg estradiol valerate, subcutaneous, once per week on Saturdays. Gender-affirming hormone therapy.
7 $316.00
74582 Psoriasis 1.0 ML Caucasian 51 Female United States
Losartan 50mg QD Flovent Inhaler HFA 220mcg BID Ventolin HFA 90mcg PRN Prenatal vitamins Calcium Munjaro
5 $316.00
73165 Psoriasis 1.0 ML Caucasian 41 Male United States
Concerta 76mg QD Bupropion 300mg QD Venlaxin 150mg QD
3 $316.00
72226 Psoriasis 1.0 ML African American Hispanic/Latino 27 Female United States
Stelara
6 $316.00
68572 Psoriasis 1.0 ML Caucasian 41 Male United States
Concerta 76mg QD Bupropion 300mg QD Venlaxin 150mg QD
6 $316.00
68230 Psoriasis 1.0 ML Hispanic/Latino 30 Female United States 2 $316.00
68630 Psoriasis 1.0 ML Caucasian 40 Male United States
Taking Skyrizi for Psoriasis Escitalopram 10mg QD
8 $316.00
68218 Psoriasis 1.0 ML Asian/Pacific Islander 48 Female United States 2 $316.00
68235 Psoriasis 1.0 ML Caucasian 60 Female United States
Ambien 10mg/QD Levothyroxine/50mcg/QD Clobetasol/PRN Hydrochlorothiazide 25mg/QD Atenolol 50mg/QD Atorvastatin 10mg/QD
3 $316.00

Human Psoriasis Serum for Immune-Mediated Inflammatory Disease Research

Our Psoriasis Serum is sourced from IRB-consented donors clinically diagnosed with psoriasis. Each sample is processed and frozen within 24 hours of collection to ensure consistency and high quality for characterising the systemic inflammation associated with psoriasis. Aliquot volumes are configured per project and reported per lot.

Why Serum for Psoriasis Research

Psoriasis is a chronic immune-mediated inflammatory disease. It is not classically autoimmune — there is no established defining autoantibody — and its pathology is driven by the IL-23 and IL-17 axis acting on keratinocytes. Serum is where the systemic dimension of that disease, and its well-documented comorbidity burden, becomes measurable.

  • Psoriasis is accompanied by systemic inflammation, and acute phase reactants such as CRP track broadly with disease extent, making serum useful for severity and comorbidity-risk biomarker research.
  • The disease carries an established association with cardiometabolic comorbidity and metabolic syndrome, so serum lipid, glycaemic, and inflammatory profiling supports research into that link rather than into skin pathology alone.
  • Circulating IL-17A itself is often present at concentrations at or below the sensitivity of routine immunoassays in psoriasis, so serum studies are generally better designed around downstream and keratinocyte-derived mediators; direct IL-17 pathway readouts are more reliably obtained from lesional skin.
  • Serum is the conventional matrix for therapeutic drug monitoring and anti-drug antibody detection, which makes psoriasis serum from biologic-treated donors directly relevant to immunogenicity assay development.
  • Because the clot is removed during processing, serum is a lower-complexity protein matrix than plasma, reducing interference in many multiplex immunoassay and mass spectrometry workflows.
  • Psoriasis and psoriatic arthritis overlap substantially, so serum from donors with and without joint involvement supports research into markers that identify arthritis risk before it becomes clinically apparent.

Donor Stratification Available

  • Severity: documented PASI, body surface area, or Investigator Global Assessment where recorded
  • Clinical phenotype: chronic plaque, guttate, inverse, pustular, or erythrodermic, including scalp, nail, and palmoplantar involvement
  • Presence or absence of psoriatic arthritis
  • Treatment status: topical therapy, phototherapy, conventional systemic agent, TNF inhibitor, IL-17 inhibitor, IL-23 inhibitor, TYK2 inhibitor, apremilast, or biologic-naive
  • Age of onset (early or late), disease duration, and family history
  • Body mass index, smoking status, and metabolic comorbidities where documented
  • Matched healthy controls available, alongside comparator inflammatory skin disease cohorts

Product Features

  • Collected from clinically confirmed psoriasis donors
  • Research Use Only (RUO)
  • Processed and frozen within 24 hours of collection
  • IRB-approved protocols with documented consent
  • Custom aliquot volumes available upon request
  • Volumes and lot-specific processing details reported per lot

De-identified Donor Data

  • Diagnosis confirmation
  • Age, sex assigned at birth, and ethnicity
  • Donor-reported allergy and infectious disease history
  • Donor-reported medication and treatment history
  • Severity and comorbidity data available upon request

Applications

  • Biomarker discovery and validation for psoriasis severity and treatment response
  • Serum cytokine, chemokine, and acute phase protein profiling
  • Cardiometabolic comorbidity and systemic inflammation research
  • Therapeutic drug monitoring and anti-drug antibody assay development for biologics
  • Proteomic and metabolomic characterisation of immune-mediated inflammation
  • Research into markers predicting progression to psoriatic arthritis
  • Immunoassay development, calibration, and matrix effect testing
  • Therapeutic candidate screening and validation with authentic patient matrix

Other Psoriasis 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

Psoriasis serum is available in standard and custom volumes. For pricing, availability, international orders, or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations. To browse other disease states and collection formats, 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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