Cystic Fibrosis (CFTR)
More than 1,000 mutations in the CFTR gene have been associated with cystic fibrosis. Most of these mutations in the CFTR gene change the production, structure, or stability of the chloride channel. All of these charevent the channel from functioning properly, which impairs the transport of chloride ions and the movement of water into and out of cells, resulting in cells lining the passageways of the lungs, pancreas, and other organs producing abnormally thick and sticky mucus. The abnormal mucus blocks the airways and glands, leading to the complications of respiratory, digestive and reproductive systems.
The assay is an in vitro PCR reaction assay for the Qualitative determination of Cystic Fibrosis (CFTR) in the human sample such as Human Whole Blood and based on Taqman detection method for Cystic Fibrosis (CFTR) with high sensitive one step QPCR kit.
All AMD kits manufactured under high quality standardization methods and unique precision and sensitive technology study compared to the most of famous and approved diagnostic commercial Cystic Fibrosis (CFTR).
AMD Cystic Fibrosis (CFTR) kit is very sensitive under our validation methods and devices.
AMD Cystic Fibrosis (CFTR) kit is very specific up to 100% for Cystic Fibrosis (CFTR) 8 mutations under our validation methods and devices.
|Product name||Technology||Package||Catalogue No|
|AMD Cystic Fibrosis (CFTR) kit||One step Real time PCR||100 reactions||KD6466212-100|