CYSTIC FIBROSIS PHENYLALANINE 508 MUTATION

A complete qPCR kit for the detection of Cystic Fibrosis phenylalanine 508 mutation

Cystic Fibrosis Phenylalanine 508 Mutation is a genetic mutation predominantly found in the human population, leading to the production of a faulty CFTR protein that affects the flow of salt and water into and out of cells. This can result in the build-up of thick, sticky mucus in the lungs and other organs, causing respiratory issues and digestive problems. It is crucial to detect this mutation early to provide timely intervention and management for individuals with cystic fibrosis, especially in the healthcare sector.

YouSeq's qPCR kit to detect Cystic Fibrosis Phenylalanine 508 Mutation allows for sensitive and specific identification of this genetic mutation, enabling early diagnosis and personalized treatment plans for affected individuals. Rapid detection of this target can lead to improved clinical outcomes, better disease management, and enhanced quality of life for patients with cystic fibrosis.