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Cystic Fibrosis, cod. AC023/25
Κλίκ για μεγέθυνση
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.

  • Detection: RDB on Strip
  • test: 25

Φόρμα Ενδιαφέροντος

Διεύθυνση: Kαισαρείας 6, 11527, Αθήνα  /  2ος Οροφος  /  Τηλ: 210 7754303 & 210 7756251  /  Φαξ: 210 7472725  /  Εmail: ndd@ndd.gr


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