Scleroderma Plasma

In Stock Samples

Lot Number Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
74801 Scleroderma 1.0 ML Caucasian 61 Female
Current: cellcept mycophenolate 2500mg QD nifedipine 30mg QD Multivitamin Previous: omeprazole 20 mg
12
74166 Scleroderma 1.0 ML Hispanic/Latino 31 Female
imuran 50 mg QD Tacrolimus 1mg 2 tab QD aygestin 10 mg QD Nutrofol QD Multivitamin
18
73118 Scleroderma 1.0 ML Caucasian 64 Female
Amlodipine 5mg QD Azelastine 137mcg BID Ciclopirox 8% solution Topically QN Dexlansoprazole 60mg BID Levothyroxine 125mcg QD Linzess 290mcg QD Losartan 25mg QD Myrbetriq 50mg QD Pilocarpine 5mg TID
17
74793 Scleroderma 1.0 ML African American 45 Female United States (US)
allopurinol // 300 mg // QD Cellcept 3 tablets in AM and PM// 500mg // BID Colchicine // 0.6 mg // prn bumex // 2mg // QD verapamil // 60 mg // BID Plaquenil // 200 mg // QD adempas // 2.5 mg // TID cymbalta // 60 mg // BID Protonix // 40mg // BID captopril // 50mg // TID micronor // 0.35 mg // QD calcitral 0.25 mg QD protonics 40mgs BID potassium supplement 10mcq PRN Bumax 2mg 3 times per week Spironolactone 25mg BID
20
74793 Scleroderma 1.0 ML African American 45 Female United States (US)
allopurinol // 300 mg // QD Cellcept 3 tablets in AM and PM// 500mg // BID Colchicine // 0.6 mg // prn bumex // 2mg // QD verapamil // 60 mg // BID Plaquenil // 200 mg // QD adempas // 2.5 mg // TID cymbalta // 60 mg // BID Protonix // 40mg // BID captopril // 50mg // TID micronor // 0.35 mg // QD calcitral 0.25 mg QD protonics 40mgs BID potassium supplement 10mcq PRN Bumax 2mg 3 times per week Spironolactone 25mg BID
1
74254 Scleroderma 1.0 ML African American 49 Male United States (US)
Mycophenolic acid 500mg 3 tablets BID Omeprazole 40mg QD Ibuterol PRN
15
73148 Scleroderma 1.0 ML Caucasian 60 Female United States (US)
Omeprazole 20mg BID Rosuvastatin 5mg QD Nebivolol 5mg QD (2.5am, 2.5pm) Baby Aspirin 81mg QD Vitamin D 5000iu QD Duloxetine 60 mg QD Zepbound Inj QW
10
70405 Scleroderma Caucasian 54 Female United States (US)
Nifedipine/60mg/QD - extended release Plaquenil/200mg/BID Metoprolol Tartrate/12.5mg/QD Atorvastatin/80mg/QD Wellbutrin/150mg/QD Triamcinolone/1%/PRN Ambien/10mg/QPM Lasix/40mg/BID Acetyloprine/10mg/QD Mycophenolate mofentil/500mg*2/BID Aspirin/81mg/BIW Multivitamin/QD Hair skin and nails supplement/QD Methotrexate Cyclovir CBD gummy no THC as needed
5

Scleroderma Plasma | High-Quality Human Plasma from Scleroderma Donors

Scleroderma Plasma is collected from donors clinically diagnosed with scleroderma (systemic sclerosis) and processed within hours of collection to preserve key analytes such as cytokines, proteins, and metabolites. This human plasma supports research focused on soluble biomarkers of vascular injury, inflammation, and fibrosis for understanding disease progression. Bulk plasma is available.

Product Features

  • Research Use Only (RUO)
  • Plasma collected from clinically confirmed scleroderma donors
  • Processed within one day of collection
  • IRB-approved protocols and informed consent
  • Custom aliquot volumes available upon request

De-identified Donor Data

  • Verified scleroderma diagnosis
  • Demographic data: age, sex assigned at birth, race/ethnicity
  • Donor-reported medications, allergies, and comorbidities
  • Additional Scleroderma-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

Scleroderma 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

  • 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 – with the exception of GMP leukopaks, all our products are research use only (RUO).

Our complete catalog can be found here: https://sanguinebio.com/products/

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 colleciton services to tailored to fit your research. For more information and request a quote, please see: https://sanguinebio.com/prospective-biospecimen-collection-services/

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 which can be found here https://sanguinebio.com/products/?pro_inventory=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: https://sanguinebio.com/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 Plasma 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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