MPS II Hunter Syndrome Whole Blood

Whole Blood samples from donors diagnosed with MPS II- Hunter syndrome are collected and processed under rigorous standards. These samples support research into iduronate sulfatase deficiency and systemic storage disease, offering insights into disease mechanisms, biomarker discovery, and therapeutic development.

Product Features

• Whole Blood isolated from clinically confirmed MPS II- Hunter syndrome donors
• Rigorous donor screening and sample quality checks
• Suitable for downstream applications such as flow cytometry, RNA-seq, ELISA, and qPCR

Donor Metadata

• Age, sex, race, medication, diagnosis method, disease severity/stage
• Optional: comorbidities, lab values, and clinical history

Applications

• Immunophenotyping
• Transcriptomics & proteomics
• Biomarker validation
• Therapeutic development and screening

Quality and Compliance

• IRB-approved protocols
• Informed donor consent
• Standardized collection and processing SOPs

Ordering & Shipping

Whole blood is available in both standard and custom volumes to meet your research needs.

International Orders: For international shipments or country-specific documentation requirements, please contact us at [email protected] to ensure compliance with your local regulations.