Whole Blood
Showing all 15 results
Cystic Fibrosis Whole Blood
Fresh Cystic Fibrosis Whole Blood – IRB-consented cystic fibrosis whole blood samples collected from clinically diagnosed donors. Ideal for systemic biomarkers and omics research.
Down Syndrome Whole Blood
Down Syndrome Whole Blood samples are obtained from donors with clinically diagnosed Down syndrome. Valuable for transcriptomic studies, immune cell phenotyping, and exploring gene expression patterns Influenzaenced by trisomy 21.
Fabry Disease Whole Blood
Fabry Disease Whole Blood – IRB-consented whole blood samples collected from donors diagnosed with Fabry Disease. Ideal for dermatology, immunology, and inflammation-based research.
Facioscapulohumeral Muscular Dystrophy Whole Blood
Facioscapulohumeral Muscular Dystrophy Whole Blood samples are obtained from donors with clinically and genetically diagnosed facioscapulohumeral muscular dystrophy (FSHD). Valuable for transcriptomic studies, immune cell profiling, and identifying gene expression patterns associated with DUX4 activation and muscular dystrophy pathology.
Friedreich’s Ataxia Whole Blood
Friedreich’s Ataxia Whole Blood samples are obtained from donors with genetically diagnosedFriedreich’s Ataxia. Valuable for gene expression studies, mitochondrial DNA analysis, and immune cell profiling in hereditary ataxia research.
Gaucher’s Disease Whole Blood
Gaucher’s Disease Whole Blood samples are obtained from donors with clinically and genetically diagnosed Gaucher’s disease. Valuable for genomic studies, enzyme assays, and immune cell profiling to explore pathogenesis and therapeutic targets.
Huntington’s Disease Whole Blood
Huntington’s Disease Whole Blood – IRB-consented whole blood samples collected from donors diagnosed with Huntington’s Disease. Ideal for dermatology, immunology, and inflammation-based research.
Mucopolysaccharidosis Whole Blood
Mucopolysaccharidosis Whole Blood samples are obtained from donors with clinically diagnosed Mucopolysaccharidosis (MPS). Valuable for genomic and transcriptomic analysis, leukocyte enzyme assays, and studying immune and inflammatory responses in lysosomal storage disorders.
Myotonic Dystrophy Whole Blood
Myotonic Dystrophy Whole Blood samples are obtained from donors with clinically diagnosed Myotonic Dystrophy (DM). Valuable for transcriptomic analysis, immune profiling, and investigating gene expression changes caused by toxic RNA repeats.
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.
Pompe Disease Whole Blood
Pompe Disease Whole Blood samples are obtained from donors with clinically diagnosed Pompe Disease (PD). Valuable for genomic and transcriptomic analysis, enzyme activity testing, and immune profiling in PD research and diagnostic studies.
Sickle Cell Disease Whole Blood
Sickle Cell Disease Whole Blood – IRB-consented whole blood samples collected from donors diagnosed with Sickle Cell Disease. Ideal for dermatology, immunology, and inflammation-based research.
Sickle Cell Trait Whole Blood
Sickle Cell Trait Whole Blood – IRB-consented whole blood samples collected from donors diagnosed with Sickle Cell Trait (HbAS). Ideal for immunology and inflammation-based research.
Spinal Muscular Atrophy Whole Blood
Spinal Muscular Atrophy Whole Blood samples are obtained from donors with clinically diagnosed Spinal Muscular Atrophy (SMA). Valuable for genomic and transcriptomic studies, SMN gene expression analysis, and immune profiling in SMA research.
Stargardt Disease Whole Blood
Stargardt Disease Whole Blood samples are obtained from donors with clinically or genetically diagnosed Stargardt Disease (STGD). Valuable for genomic and transcriptomic studies to identify ABCA4 mutations and molecular pathways involved in STGD pathogenesis.