Polycystic Kidney Disease Whole Blood

<h2>Polycystic Kidney Disease Whole Blood for Research</h2>
Polycystic kidney disease (PKD) is a genetic disorder caused by PKD1 or PKD2 mutations, leading to progressive cyst formation and declining kidney function. Sanguine collects fresh whole blood from IRB-consented donors with a clinically confirmed PKD diagnosis for nephrology and genetic disease research.
<h3>Product Features</h3>
<ul><li>Fresh whole blood from clinically diagnosed PKD 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 PKD1/PKD2 genotype and kidney function where available</li><li>Demographics: age, sex assigned at birth, ethnicity</li><li>Relevant medical and family history</li></ul>
<h3>Applications</h3>
<ul><li>PKD1/PKD2 gene variant research</li><li>Cystogenesis and kidney function biomarker studies</li><li>Gene expression and transcriptomic analysis</li><li>Vasopressin receptor antagonist therapy response research</li></ul>
<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>
PKD 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.