Cell line was derived from a single caucasian male donor diagnosed with Cystic Fibrosis. Cystic fibrosis is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) protein, which is involved in mucus production. This genetic disorder primarily affects the lungs, pancreas, liver, kidneys, and intestines. Vial contains approximately 500,000 cells. Shipped with dry ice.
| Documents & Links for Human Cystic Fibrosis iPS Cells | |
| Vendor Page | Human Cystic Fibrosis iPS Cells at Cellular Engineering Technologies |
| Documents & Links for Human Cystic Fibrosis iPS Cells | |
| Vendor Page | Human Cystic Fibrosis iPS Cells |