Secondary Progressive Multiple Sclerosis Whole Blood

Fresh Secondary Progressive Multiple Sclerosis Whole Blood

Secondary Progressive Multiple Sclerosis Whole Blood is collected from IRB-consented donors with clinically confirmed Secondary Progressive Multiple Sclerosis (SPMS). These fresh samples are ideal for developing early detection diagnostics, immunological studies, and understanding disease progression.

Product Features

  • Fresh SPMS whole blood from clinically diagnosed donors
  • Custom tubes and anticoagulants available
  • Collected and shipped same-day for maximum freshness
  • Research Use Only (RUO)

De-identified Donor Data

  • Confirmed SPMS diagnosis by physician or specialist
  • Demographic details: age, sex assigned at birth, ethnicity
  • Medical history including allergies and infectious disease status

Applications

  • Immunophenotyping of immune cell populations in SPMS
  • Gene expression and transcriptomic analysis
  • Inflammatory marker and cytokine profiling
  • Drug response and mechanism-of-action studies

Compliance and Quality

  • IRB-approved protocols and electronic informed consent
  • HIPAA-compliant data management

Ordering and Customization

Secondary Progressive Multiple Sclerosis whole blood is available in a range of standard and custom volumes. For international orders or documentation requirements, please email learnmore@sanguinebio.com to ensure compatibility with your country’s regulations.

Secondary Progressive Multiple Sclerosis Publications

Whole Blood

Frequently Asked Questions

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What is the lead time for fresh whole blood delivery and can I pick up locally?

1 Answer

Collected and shipped same-day – local pickup may be available. For more information, request a quote or contact: LearnMore@sanguinebio.com

YES – The same-day program processes and ships samples on the day of collection, ensuring delivery well within 48 hours for the designated service areas.

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Need a custom Whole Blood 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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