Asthma Plasma

In Stock Samples

Lot # Condition Volume Race/Ethnicity Age Gender Country of Collection Medications Vials Price Action
67201 Asthma 1.0 ML African American 29 Male
Albuterol PRN
4 $316.00
68227 Asthma 1.0 ML Caucasian 47 Male
Albuterol dispenser Clobetasol propionate
16 $316.00
65945 Asthma 1.0 ML Other 63 Female
levothyroxine 1.0 mg
8 $316.00
64573 Asthma 1.0 ML African American 29 Male
Albuterol PRN
5 $316.00
56037 Asthma 1.0 ML Caucasian 75 Female 2 $316.00
69089 Asthma 1.0 ML Caucasian 64 Male United States (US)
fluticasone proprionate 60mcg QD albuterol inhaler PRN emergency inhaler PRN
13 $316.00
68232 Asthma 1.0 ML Other 41 Male United States (US)
albuterol inhaler PRN
8 $316.00

Asthma Plasma | High-Quality Human Plasma from Asthma Donors

Asthma Plasma is collected from donors clinically diagnosed with asthma 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 asthma pathophysiology.

Product Features

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

De-identified Donor Data

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

Asthma 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

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Do samples come with donor screening reports?

1 Answer

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/

YES – Certificate of analysis is available upon request.

Lead times vary from ready to ship inventory to prospective studies.

International shipping is available. We also work with a number of distributors. Contact us to discuss options at learnmore@sanguinebio.com.

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/

You can request a quote on this page or contact us at learnmore@sanguinebio.com. https://sanguinebio.com/request-quote/

NO – no minimum order requirements.

For bulk pricing inquiries, please contact: LearnMore@sanguinebio.com

YES – Bulk plasma is available: https://sanguinebio.com/product/human-bulk-plasma/

YES – The “Specify I/E Criteria” service allows you to define specific inclusion/exclusion criteria including lifestyle restrictions.

YES – Sanguine offers longitudinal collections.

YES – Sanguine offers matched samples across multiple matrices and age-matched controls.

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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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