Thyroid Eye Disease Serum

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
70181 Thyroid Eye Disease 1.0 ML Caucasian 77 Male United States
Tepezza Methimazole QD M-F Losartan 25mg QD Atorvastatin 20mg QD Sertraline QD Finasteride 1mg QD
5 $667.00
69369 Thyroid Eye Disease 1.0 ML Caucasian 58 Female United States
Levothyroxine Prescribed eye drops
4 $667.00
69462 Thyroid Eye Disease 1.0 ML Caucasian 55 Female United States
Synthroid QD Zetia QD Protonix QD Allegra D QD Lunesta prn Gabapentin QD Flexeril Nightly
6 $667.00
69370 Thyroid Eye Disease 1.0 ML African American 57 Female United States
Synthroid 88 mcg QD Sertraline 50mg QD Zyrtec OTC QD Amlodipine 10 mg QD
6 $667.00
69341 Thyroid Eye Disease 1.0 ML Caucasian 46 Female United States
Levothyroxine .112, GLP-1, magnesium, Tepezza Synthroid 112 mcg QD Phentermine 37.5 mg QD Celebrex 100 mg PRN Refresh eye drops PRN Systane eye drops PRN
6 $667.00
69444 Thyroid Eye Disease 1.0 ML Caucasian 53 Female United States
Synthroid, colanzepin depakote metoprolol vraylar
6 $667.00

Human Thyroid Eye Disease Serum for Research

Our Thyroid Eye Disease Serum is sourced from IRB-consented donors clinically diagnosed with Thyroid Eye Disease (TED). Each sample is processed and frozen within 24 hours of collection to ensure consistency and high quality for disease-specific and immunological studies focused on TED.

Product Features

  • Collected from clinically confirmed Thyroid Eye Disease donors
  • Research Use Only (RUO)
  • IRB-approved protocols with documented consent

De-identified Donor Data

  • Diagnosis confirmation
  • Age, sex assigned at birth, and ethnicity
  • Donor-reported medical history and comorbidities

Applications

  • Biomarker discovery for thyroid eye disease
  • Serum cytokine and protein profiling
  • Therapeutic candidate screening and validation

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

Thyroid Eye Disease serum 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

  • 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.

More Information