Immunohistochemistry of CFTR in native tissues and primary epithelial cell cultures

J Cyst Fibros. 2004 Aug:3 Suppl 2:37-41. doi: 10.1016/j.jcf.2004.05.008.

Abstract

Studies on CFTR protein expression and localization in native tissues or in primary cultures of human epithelial cells are scarce due to the intrinsic instability of this protein, its low expression in most tissues and also to technical difficulties. However, such data are of the highest importance to understand the pathophysiology of CF. The purpose of this article is to outline several assays for the characterization of primary epithelial cultures and to review different CFTR immunostaining protocols.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cell Culture Techniques
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / immunology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / immunology*
  • Epithelial Cells
  • Gene Expression / immunology*
  • Humans
  • Immunohistochemistry / methods*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator