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ITEM#: 3042-50205A
MFR#: 502-05A
HBEpC provide an excellent model system to study all aspects of epithelial function and disease, particularly those related to airway viral infections, as well as tissue repair mechanisms, signaling changes and potential treatments relevant to lung i
| Product Name | Description | Item# | QTY | |
|---|---|---|---|---|
Human Bronchial Epithelial Cells (HBEpC) 500,000 cryopreserved cells
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Human Bronchial Epithelial Cells (HBEpC) 500,000 cryopreserved cells | 3042-C12640 | EA | |
Human Bronchial Epithelial Cells (HBEpC) 1 million cells per pellet
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Human Bronchial Epithelial Cells (HBEpC) 1 million cells per pellet | 3042-C14063 | EA | |
16HBE14o-Human Bronchial Epithelial Cell Line
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16HBE14o- is a human bronchial epithelial cell line isolated from a 1-year old male heart-lung patient and immortalized with the origin-of-replication defective SV40 plasmid (pSVori-). The cell line retains characteristic features of normal different | 3042-SCC150 | EA | |
CFBE41o- Human CF Bronchial Epithelial Cell Line CFBE41o- human CF bronchial epithelial cell line was derived from a cystic fibrosis patient homozygous for the DeltaF508 CFTR mutation.
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Cystic Fibrosis (CF) is a lethal autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene which functions as a cAMP-activated and phosphorylated-regulated Cl channel. The predominant mutation in the CF | 3042-SCC151 | EA | |
Human Tracheal Epithelial Cells: HTEpC, adult
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HTEpC provide a useful model system to study all aspects of epithelial function and disease, particularly those related to airway viral infections, as well as tissue repair mechanisms, signaling changes and potential treatments relevant to lung injur | 3042-50405A | EA |