Gaucher Disease

Gaucher Disease

ViennaLab´s Gaucher Disease StripAssay® offers an easy way to identify the most

frequent mutations (8) and recombinant alleles in the GBA gene.

  • Gaucher Disease is the most common inherited lysosomal storage disorder
  • The disease is caused by glucocerebrosidase deficiency due to mutations
  • Enlarged spleen and liver, anemia, thrombocytopenia, bone lesions, bone marrow suppression, hyperpigmentation and neurologic complications

  • Enzyme replacement therapy may offer clinical amelioration and an improvedquality of life

The ViennaLab Gaucher Disease StripAssays®
• are based on reverse-hybridization of biotinylated PCR products
• combine probes for mutations and controls in a parallel array of allele-specific oligonucleotides
• work with immobilized oligos on a teststrip
• show mutations by enzymatic color reaction easily visible to the naked eye

Gaucher Disease

ProductCat.CapacityApplication
Gaucher Disease StripAssay®4-25020 TestsDetection of 8 mutations and two recombinant alleles in the glucocerebrosidase (GBA) gene

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