Optimized growth conditions for trans-well inserts have not been established. It is suggested to grow these cells on ECM-coated T75 tissue culture flasks as per the user protocol. However, 16HBE14o- cells seem to grow well on fibronectin-coated inserts containing bovine serum albumin. For a detailed protocol reference, the following publication may be useful: Eur J Pharm Biopharm. 2011 Apr;77(3):398-406. An in vitro triple cell co-culture model with primary cells mimicking the human alveolar epithelial barrier. PMID: 21056660.
SCC150
16HBE14o- Human Bronchial Epithelial Cell Line
Human
Synonym(s):
16HBE, 16-HBE, 16HBEo-, 16-HBEo, 16-HBE14o
About This Item
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Product Name
16HBE14o- Human Bronchial Epithelial Cell Line, 16HBE14o- human bronchial epithelial cell line is widely used to model barrier function of the airway epithelium and to study respiratory ion transport as well as the function of CFTR.
biological source
human
technique(s)
cell based assay: suitable
cell culture | mammalian: suitable
General description
Cell Line Description
Application
Quality
• Cells are tested by PCR and are negative for HPV-16, HPV-18, Hepatitis A, C, and HIV-1 & 2 viruses as assessed by a Human Essential CLEAR panel by Charles River Animal Diagnostic Services.
• Cells are negative for mycoplasma contamination.
• Each lot of cells is genotyped by STR analysis to verify the unique identity of the cell line.
Storage and Stability
Other Notes
Disclaimer
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
16HBE14o- human bronchial epithelial cells used to model respiratory epithelium for the research of cystic fibrosis, viral pulmonary pathology (SARS-CoV), asthma, COPD, effects of smoking and air pollution. See over 5k publications.
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Are there any issues with the cell growth of 16HBE14o- cells on 0.4 and 3 micron pore size trans-ell inserts? The cells were seeded at 1x10^5 cells per insert with an area of 0.47 cm^2. After growing the monolayer for two days and removing the medium from the apical side, it has been over a week under ALI conditions, but the cells do not have cilia, and the TEER has not increased.
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