Myelofibrosis Serum

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
74104 Myelofibrosis 1.0 ML Caucasian 61 Male
Jakafi 15 mg po BID Atorvastatin 10 mg po QD Aspirin 81 mg po QD
8 $667.00
74071 Myelofibrosis 1.0 ML Caucasian 56 Female United States (US)
Jakofi 10 mg po BID
6 $667.00
74105 Myelofibrosis 1.0 ML Caucasian 56 Female United States (US)
Metoprolol 50 mg – once daily (QD) Omeprazole 40 mg – once daily (QD) Trazodone 100 mg – once daily (QD) Aspirin 81 mg – once daily (QD) Calcium + Vitamin D supplement – once daily
8 $667.00
74092 Myelofibrosis 1.0 ML Caucasian 68 Male United States (US)
Eliquis Aspirin 81 mg QD Atorvastatin 5 mg QD Hydrochlorthiazide 12.5 mg QD Lisinopril 2.5 mg QD Hydroxyurea 1000 mg x4days; 1500 mg x 3 days
6 $667.00
74079 Myelofibrosis 1.0 ML Caucasian 55 Male United States (US)
Lumigan Eye Drops Amlodipine 10 mg po QD
8 $667.00

Human Myelofibrosis Serum for Research

Our Myelofibrosis Serum is sourced from IRB-consented donors clinically diagnosed with myelofibrosis. Each sample is processed and frozen within 24 hours of collection to ensure consistency and high quality for studies to characterize markers associated with disease severity.

Product Features

  • Collected from clinically confirmed myelofibrosis 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 allergy and infectious disease history

Applications

  • Biomarker discovery for myelofibrosis
  • 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

Myelofibrosis 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

Showing 1–12 of 24 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.

1 2
×

Ask a Question

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