Psoriatic Arthritis Plasma

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
74700 Psoriatic Arthritis 1.0 ML Caucasian 69 Female United States
Otezla 30 mg BID Bupropion 150 mg QD Fluoxetine 120 mg QD Atorvastatin 5 mg QD
20 $495.00
74572 Psoriatic Arthritis 1.0 ML Caucasian 65 Male United States
Lipitor 10 mg QD Methotrexate 15 mg QW Folic Acid 1 mg QD Wegovy 1.7 mg QW
14 $495.00
72225 Psoriatic Arthritis 1.0 ML Caucasian 68 Female United States
Methylprednisolone, Doxycycline and Benzonatate,Cosentyx, Methotrexate, Folic acid,Benazepril, Levothyroxine, Sildenafil, Ambrisentan, Amitriptyline, Zoloft, Wellbutrin, Quetiapine, Metronidazole cream
18 $495.00
69582 Psoriatic Arthritis 1.0 ML Caucasian 51 Female United States 16 $495.00
69604 Psoriatic Arthritis 1.0 ML Caucasian 54 Female United States
Rinvoq methotrexate folic acid gabapentin
16 $495.00
69603 Psoriatic Arthritis 1.0 ML Caucasian 61 Female United States 16 $495.00
68216 Psoriatic Arthritis 1.0 ML Caucasian 49 Male United States
Bimzelx 160 mg/mL subcutaneous syringe
15 $495.00
68574 Psoriatic Arthritis 1.0 ML Caucasian 60 Female United States
Taltz 80mg/mL Wegovy 2.4mg/0.75 mL Zoloft Zepbound 15mg/0.5 mL
15 $495.00
80290 Psoriatic Arthritis 1.0 ML Caucasian 68 Female United States
Methylprednisolone, Doxycycline and Benzonatate,Cosentyx, Methotrexate, Folic acid,Benazepril, Levothyroxine, Sildenafil, Ambrisentan, Amitriptyline, Zoloft, Wellbutrin, Quetiapine, Metronidazole cream
20 $495.00

Psoriatic Arthritis Plasma for Immune-Mediated Inflammatory Disease Research

Psoriatic Arthritis Plasma is collected from IRB-consented donors clinically diagnosed with psoriatic arthritis and processed within one day of collection to preserve labile analytes such as cytokines, proteins and metabolites. Psoriatic arthritis is an immune-mediated inflammatory spondyloarthritis associated with psoriasis. It is characteristically seronegative, and framing it as an autoantibody-driven autoimmune disease misrepresents its biology.

What Psoriatic Arthritis Plasma Reveals

  • Psoriatic arthritis is centred on the IL-23 and Th17 axis rather than on autoantibody production. That mechanism is validated by therapy: IL-17A inhibitors, IL-23 p19 inhibitors and IL-12/23 inhibitors are all effective, alongside TNF inhibitors and JAK inhibitors. Plasma is the practical matrix for the circulating mediators of that axis.
  • Rheumatoid factor and anti-CCP antibodies are typically absent, which is the key serological distinction from rheumatoid arthritis. Plasma from psoriatic arthritis donors is therefore valuable as a seronegative inflammatory arthritis comparator in assay specificity work.
  • Bone remodelling in psoriatic arthritis is bidirectional: erosion coexists with new bone formation, periostitis, enthesophytes and ankylosis, unlike the purely erosive pattern in rheumatoid arthritis. Circulating bone turnover mediators, including the RANKL and osteoprotegerin axis and Wnt pathway regulators such as Dickkopf-1, reflect that dual biology.
  • CRP is frequently normal despite clinically active disease, which is a well-recognised limitation. This is exactly why plasma-based multiplex cytokine, chemokine and proteomic approaches are being pursued as more sensitive activity measures.
  • Matrix metalloproteinase-3, calprotectin and angiogenic mediators such as VEGF reflect synovial and entheseal tissue processes that are otherwise only accessible by imaging or biopsy.
  • The disease is multi-domain, spanning peripheral arthritis, enthesitis, dactylitis, axial involvement, skin psoriasis and nail disease, with an HLA-B27 association in axial presentations. Plasma from domain-annotated donors lets circulating markers be linked to specific disease compartments rather than to a single global label.

Donor Stratification Available

  • Clinical domains involved: peripheral arthritis pattern, enthesitis, dactylitis, axial disease, nail disease
  • Disease activity where documented, including DAPSA or minimal disease activity status, tender and swollen joint counts, and CRP or ESR
  • Skin disease severity where documented, including PASI or body surface area, and psoriasis subtype
  • Treatment status: treatment-naive, methotrexate or other conventional DMARD, TNF inhibitor, IL-17 inhibitor, IL-23 or IL-12/23 inhibitor, JAK inhibitor, or PDE4 inhibitor
  • Serology and genetics where documented: RF and anti-CCP negativity confirmed, HLA-B27 status, radiographic erosion or new bone formation
  • Matched healthy controls available, along with psoriasis-without-arthritis and rheumatoid arthritis donors for comparison

Product Features

  • Research Use Only (RUO)
  • Plasma collected from clinically confirmed psoriatic arthritis donors
  • Processed within one day of collection
  • Anticoagulant selection (EDTA, citrate, heparin) available on request
  • IRB-approved protocols and informed consent
  • Custom aliquot volumes available upon request; volumes reported per lot

De-identified Donor Data

  • Verified psoriatic arthritis diagnosis
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Additional psoriatic arthritis-specific metadata available on request

Applications

  • IL-23/Th17 axis cytokine profiling, including IL-17A, IL-23, TNF and IL-6
  • Bone turnover and Wnt pathway marker research, including RANKL, osteoprotegerin and Dickkopf-1
  • MMP-3, calprotectin and tissue remodelling marker quantification
  • Disease activity biomarker discovery in CRP-normal active disease
  • Seronegative versus seropositive inflammatory arthritis differential marker studies
  • Plasma proteomics and metabolomics
  • Biologic and JAK inhibitor pharmacodynamic and response biomarker research
  • Therapeutic target validation and immunoassay qualification in a disease-state matrix

Other Psoriatic Arthritis 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

Psoriatic arthritis plasma 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 plasma page.

Protocols & Documentation

  • Plasma Isolation

    Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.

    Download
  • Informed Consent Form (ICF)

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

Plasma

Frequently Asked Questions

Showing 1–12 of 31 results

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.

1
×

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.

More Information