Nonalcoholic Fatty Liver Disease Plasma
About: Nonalcoholic Fatty Liver Disease Plasma samples are collected from donors diagnosed with Nonalcoholic Fatty Liver Disease (NAFLD). Suitable for analyzing circulating biomarkers such as ALT, AST, adipokines, cytokines, and markers of insulin resistance and liver fibrosis.
Nonalcoholic Fatty Liver Disease Plasma | High-Quality Human Plasma from Nonalcoholic Fatty Liver Disease Donors
Nonalcoholic Fatty Liver Disease Plasma is collected from donors clinically diagnosed with Nonalcoholic Fatty Liver Disease and processed within hours of collection to preserve key analytes such as cytokines, proteins, and metabolites. This human plasma supports research focused on inflammatory pathways, immune profiling, and biomarker discovery in nonalcoholic fatty liver disease pathophysiology.
Product Features
- Research Use Only (RUO)
- Plasma collected from clinically confirmed Nonalcoholic Fatty Liver Disease donors
- Processed within one day of collection
- IRB-approved protocols and informed consent
- Custom aliquot volumes available upon request
De-identified Donor Data
- Verified Nonalcoholic Fatty Liver Disease diagnosis
- Demographic data: age, sex assigned at birth, race/ethnicity
- Donor-reported medications, allergies, and comorbidities
- Additional nonalcoholic fatty liver disease-specific metadata available
Applications
- Biomarker discovery and validation
- Cytokine and inflammation profiling
- Metabolomics and proteomics studies
- Therapeutic response research
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 and Customization
Nonalcoholic Fatty Liver Disease plasma is available in standard and custom volumes. For international orders or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations.
Protocols & Documentation
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Download
Plasma Isolation
Protocol for plasma separation from anticoagulated whole blood, including processing, storage, and traceability requirements.
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Informed Consent Form (ICF)
Available upon request — confirms donor consent for research use and downstream commercialization.
Plasma
Frequently Asked Questions
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All our samples have self-reported infectious disease testing and verified clinical diagnosis. Many of our samples have the option of electronic medical records provided and our prospective collection offers the opportunity for patient reported outcomes and surveys. Learn more here. https://sanguinebio.com/patient-reported-outcomes-pro-surveys-questionnaires/
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YES – Certificate of analysis is available upon request.
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Lead times vary from ready to ship inventory to prospective studies.
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International shipping is available. We also work with a number of distributors. Contact us to discuss options at learnmore@sanguinebio.com.
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We have several ordering methods. You can order directly online with a PO or credit card or contact us to have a sales specialist help with your order. https://sanguinebio.com/request-quote/
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You can request a quote on this page or contact us at learnmore@sanguinebio.com. https://sanguinebio.com/request-quote/
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NO – no minimum order requirements.
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For bulk pricing inquiries, please contact: LearnMore@sanguinebio.com
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YES – Bulk plasma is available: https://sanguinebio.com/product/human-bulk-plasma/
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YES – The “Specify I/E Criteria” service allows you to define specific inclusion/exclusion criteria including lifestyle restrictions.
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YES – Sanguine offers longitudinal collections.
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YES – Sanguine offers matched samples across multiple matrices and age-matched controls.
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.