Idiopathic Pulmonary Fibrosis Whole Blood

<h2>Idiopathic Pulmonary Fibrosis Whole Blood for Research</h2>
Idiopathic pulmonary fibrosis (IPF) is a progressive, fibrosing lung disease of unknown cause, studied through fibrotic pathway and lung function biomarkers. Sanguine collects fresh whole blood from IRB-consented donors with a clinically confirmed IPF diagnosis for pulmonology and fibrosis research.
<h3>Product Features</h3>
<ul><li>Fresh whole blood from clinically diagnosed IPF donors</li><li>Custom anticoagulants and collection tubes available</li><li>Same-day collection and shipment</li><li>Research Use Only (RUO)</li></ul>
<h3>De-identified Donor Data</h3>
<ul><li>Physician-confirmed diagnosis, including pulmonary function test results where available</li><li>Demographics: age, sex assigned at birth, ethnicity, smoking history</li><li>Relevant medical and treatment history</li></ul>
<h3>Applications</h3>
<ul><li>Fibrotic pathway and biomarker research</li><li>Lung function decline studies</li><li>Gene expression and transcriptomic analysis</li><li>Antifibrotic therapy response research</li></ul>
<h3>Also Available</h3>
Looking for our general pulmonary fibrosis product? See our <a href=”https://sanguinebio.com/product/pulmonary-fibrosis-whole-blood/”>Pulmonary Fibrosis Whole Blood</a> product.
<h3>Compliance and Quality</h3>
<ul><li>IRB-approved protocols and electronic informed consent</li><li>HIPAA-compliant donor data handling</li></ul>
<h3>Ordering and Customization</h3>
IPF whole blood is available in standard and custom volumes. Email <a href=”mailto:learnmore@sanguinebio.com”>learnmore@sanguinebio.com</a> for international orders or documentation requirements.