Cystic Fibrosis PCR

Cystic Fibrosis PCRCystic Fibrosis is the most common life-limiting autosomal recessive disorder in the Caucasion population.

ViennaLab offers population tailored Cystic Fibrosis PCR with CF StripAssay including 46 common CFTR mutations and the Poly T variant 5T/7T/9T in intron 8.

Cystic Fibrosis 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

The ViennaLab Cystic Fibrosis 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

Cystic Fibrosis

ProductCat.CapacityApplication
Cystic Fibrosis StripAssay®4-44010 TestsDetection of 38 mutations + 1 Polymorphism
Cystic Fibrosis StripAssay®4-41010 TestsDetection of 34 common CFTR mutations and the IVS8 variants 5T/7T/9T
Cystic Fibrosis StripAssay® TUR4-42010 TestsDetection of 24 common DFTR mutations and the IVS8 variants 5T/7T/9T
Cystic Fibrosis StripAssay® GER4-43010 TestsDetection of 31 common CFTR mutations

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Total Overview All Viennalab StripAssays