Alzheimer disease is a neurodegenerative disorder characterized by progressive dementia, loss of cognitive abilities. This disease cell model has a mutation (A673T) on APP gene , belongs to FAD, a familial early-onset form of Alzheimer disease. Generating pluripotent stem cells from fibroblasts, then differentiate into cortical neurons . This disease cell model provides a platform to explore disease mechanisms in AD.
Specifications | |
---|---|
Organ System | Central Nervous System |
Disease | Alzheimer's Disease (AD) |
Target Gene | APP |
Gene Function | Encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. |
Mutation | A673T |
Phenotype | Threefold higher Aβ levels in homozygous, and twofold higher Aβ levels in heterozygous APPSwe mutant |
Source | Fibroblasts |
Cellular Assays | Immunocytochemistry, FACS, Amyloid-β measurements |
For Research Use Only. Not For Clinical Use.