CR1008-500 – Human Alzheimer’s Presenilin-1 Mutation iPSCs, ~500,000 cells

For more information, click here.

The cell line was derived from a single male with Alzheimer’s disease, with onset occurring at the age of 45. The donor cells were collected via skin biopsy of the forearm antemortem. The cell morphology is fibroblast-like.

Mutations in the PSEN1 gene, encoding presenilin-1 (PS1), are the most common common cause of familial Alzheimer’s disease (FAD). PS1 is the catalytic subunit of y-secretase, an intramembranous protease that cleaves various type 1 transmembrane proteins, notably the amyloid precursor protein (APP) and Notch.

Vial contains approximately 500,000 cells. Shipped with dry ice.