Genetic Disorders

Cystic Fibrosis, cod. AC023/25

Cod. AC023/25

KIT Name: Cystic Fibrosis

Description: The AC023/25 device provides reagents for the identification of variants in the gene CFTR (Cystic Fibrosis Transmembrane Conductance Regulator), through the amplification of target sequences, reverse-hybridization and color development. Cystic Fibrosis is due to an anomaly in the CFTR protein (Cystic Fibrosis Transmembrane Conductance Regulator) placed in the apical membrane of epithelial cells. Its function is related to the regulation of electrolytic exchange.

Extraction: AA1001

Detection: RDB on Strip

test: 25

Leaflet Cystic Fibrosis Kits Download
Certificate VEQ 2018 - CF Download
Certificate VEQ 2017 - CF Download
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