
T5424 Human Primary DF508/N1303K Cystic Fibrosis Bronchial Epithelial Cells by ABM — compound heterozygous CFTR mutations (ΔF508/N1303K), 5×10⁵ cells/1.0 ml, BSL-II. Requires PriCoat™ T25 Flasks and PriGrow TM5424 medium. For CF disease modeling and CFTR modulator research. MTA required.