VIENNALAB - Established innovations in diagnostics

Cystic Fibrosis (CF) is the most common life-limiting autosomal recessive disorder in the Caucasian population. ViennaLab offers population-tailored     CF StripAssays® including 46 common CFTR mutations and the polyT variant 5T/7T/9T in intron 8.

CF StripAssays®

  • The disease incidence is estimated to be 1 in 2,500 to 4,000 live births
  • Affected children commonly experience decreased pulmonary function along with persistent respiratory infections, pancreatic insufficiency and malnutrition
  • Clinical manifestations vary by severity of the underlying CFTR mutations, ranging from classical CF to the milder forms of CFTR-related disorders
  • In newborn screening CFTR genotyping enables early diagnosis and minimizes emotional stress for parents

Product Details

CF StripAssay® ref4-410
CF StripAssay® TUR ref4-420
CF StripAssay® GER ref4-430