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Expansion of cultures of human tracheal epithelium with maintenance of differentiated structure and function

We have developed a technique for expanding primary cultures of human tracheal epithelium while minimizing loss of differentiated structure and function. Cells were seeded at 2 × 104 cells/cm2 into T75 flasks and trypsinized when approximately 80% confluent. The dispersed cells were then passaged at...

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Bibliografski detalji
Glavni autori: Jonathan H. Widdicombe, Lorne A. Sachs, Joby L. Morrow, Walter E. Finkbeiner
Format: Artigo
Jezik:Inglês
Izdano: Taylor & Francis Group 2005-08-01
Serija:BioTechniques
Online pristup:https://www.future-science.com/doi/10.2144/05392RR02
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