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Gaucher’s Disease PBMC
Gaucher’s Disease PBMC samples are isolated from donors with genetically confirmed Gaucher’s disease. Ideal for studying lysosomal storage dysfunction, macrophage activation, and immune alterations associated with glucocerebrosidase deficiency.
Gaucher’s Disease Plasma
Gaucher’s Disease Plasma samples are collected from donors diagnosed with Gaucher’s disease. Suitable for analyzing biomarkers such as chitotriosidase, CCL18, and glucosylsphingosine (Lyso-Gb1), which reflect disease activity and treatment response.
Gaucher’s Disease Serum
Gaucher’s Disease Serum samples are derived from donors with confirmed Gaucher’s disease. Useful for measuring enzyme activity, inflammatory mediators, and metabolic profiles linked to systemic involvement in lysosomal storage disorders.
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.