Autoimmune Hepatitis Whole Blood is collected from donors with clinically confirmed autoimmune hepatitis. Suitable for transcriptomic analysis, immune cell profiling, and genetic studies related to autoimmune liver disease.

Cirrhosis Whole Blood

Cirrhosis Whole Blood samples are obtained from donors with clinically diagnosed cirrhosis. Valuable for comprehensive immune profiling, gene expression analysis, and exploring hematologic changes linked to chronic liver disease.

Nonalcoholic Fatty Liver Disease Whole Blood

Nonalcoholic Fatty Liver Disease Whole Blood samples are obtained from donors with clinically diagnosed Nonalcoholic Fatty Liver Disease (NAFLD). Valuable for transcriptomic and genomic analysis, immune profiling, and identifying systemic contributors to metabolic liver disease.

Nonalcoholic Steatohepatitis Whole Blood

Nonalcoholic Steatohepatitis Whole Blood samples are obtained from donors with clinically diagnosed Nonalcoholic Steatohepatitis (NASH). Valuable for gene expression studies, immune cell profiling, and identifying molecular signatures driving NASH-related liver damage.

PFIC Whole Blood

PFIC Whole Blood samples are obtained from donors with clinically diagnosed Progressive Familial Intrahepatic Cholestasis (PFIC). Valuable for genomic and transcriptomic studies, immune cell profiling, and identifying gene mutations and systemic responses involved in PFIC.

Polycythemia Vera Whole Blood

Polycythemia Vera Whole Blood samples are obtained from donors with clinically diagnosed Polycythemia Vera (PV). Valuable for genomic and transcriptomic analysis, JAK2 mutation detection, and immune profiling in this chronic myeloproliferative neoplasm.

Primary Biliary Cholangitis Whole Blood

Primary Biliary Cholangitis Whole Blood – IRB-consented whole blood samples collected from donors diagnosed with Primary Biliary Cholangitis (Cirrhosis). Ideal for dermatology, immunology, and inflammation-based research.

Wilson’s Disease Whole Blood

Wilson’s Disease Whole Blood samples are obtained from donors with clinically diagnosed Wilson’s Disease (WD). Valuable for genomic and transcriptomic studies, ATP7B mutation analysis, and immune profiling in this inherited metabolic disorder.