VIENNALAB - Established innovations in diagnostics

α-and β-thalassemia are severe forms of anemia caused by specific mutations in the globin genes of the haemoglobin molecule. Globin StripAssays®, optimized for regional prevalences, identify the most relevant mutations.


  • Thalassemias belong to the most frequent hereditary diseases posing a major public health problem.
  • They are especially frequent in Mediterranean countries, Africa, the Middle East, South-East Asia, and the Indian subcontinent.
  • Due to demographic changes during the last decades their incidence has increased worldwide.
  • Up-to-date, no ultimate cure apart from bone marrow transplantation is available.
  • Therefore, Health Authorities focus on screening programs.


Product Details

ß-Globin StripAssay® MED ref4-130
ß-Globin StripAssay® IME ref4-140
ß-Globin StripAssay® SEA ref4-150
α-Globin StripAssay® ref4-160
ß-Thal Modifier StripAssay® ref4-170