Axial Spondyloarthritis Synovial Fluid
About: Axial Spondyloarthritis Synovial Fluid is collected from donors with clinically confirmed axial spondyloarthritis (axSpA). Suitable for cytokine profiling, immune cell analysis, and biomarker research related to spondyloarthropathies.
Axial Spondyloarthritis Synovial Fluid for Research
Axial Spondyloarthritis Synovial Fluid samples are collected from clinically confirmed axial spondyloarthritis (axSpA) donors. These high-quality synovial fluid samples support research in inflammation, joint degeneration, and autoimmune pathways.
Product Features
- Research Use Only (RUO), fresh or frozen synovial fluid
- Samples are frozen (if requested) within 4 hours of collection
- Clinically confirmed Axial Spondyloarthritis donors
- Collected by licensed clinicians under aseptic conditions
- Processed and shipped same-day where applicable
- IRB-approved protocols and electronic informed consent
De-identified Donor Data
- Verified diagnosis of Axial Spondyloarthritis
- Donor demographics: age, sex assigned at birth, race/ethnicity
- Self-reported medication history and affected joints
- Disease activity and clinical history available upon request
Applications
- Cellular and cytokine profiling of synovial fluid
- Transcriptomic and proteomic analysis
- Biomarker discovery and immunophenotyping
- Therapeutic response studies and drug target validation
Quality and Compliance
- IRB-approved collections and SOP-driven processing
- 21 CFR Part 11-compliant electronic informed consent
- HIPAA-compliant donor data management
Ordering & Shipping
Axial Spondyloarthritis Synovial Fluid samples can be shipped ambient, refrigerated, or on dry ice. For orders outside the United States or regulatory documentation, please contact learnmore@sanguinebio.com.
Protocols & Documentation
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Frequently Asked Questions
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Need a custom biospecimens cohort?
Our scientific team can scope prospective collections with donor-specific I/E criteria, typically starting within 2 weeks of agreement.