Anion transport and 2,3-diphosphoglycerate in cystic fibrosis red blood cells

Berghout, Alexander G.R.V.; Bender, S.W.

doi:10.1203/00006450-198410000-00021

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Anion transport and 2,3-diphosphoglycerate in cystic fibrosis red blood cells

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Berghout, Alexander G.R.V.
Department of Cell Physiology, Max Planck Institute of Biophysics, Max Planck Society;

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Berghout, A. G., & Bender, S. (1984). Anion transport and 2,3-diphosphoglycerate in cystic fibrosis red blood cells. Pediatric Research, 18(10), 1017-1020. doi:10.1203/00006450-198410000-00021.

Cite as: https://hdl.handle.net/21.11116/0000-0008-CD55-2

Abstract

The monovalent and divalent anion transport in red blood cells from patients with cystic fibrosis and controls is not significantly different. The protein pattern of the erythrocyte membrane, as seen by sodium dodecyl sulfate-polyacrylamide gel electropherograms, is similar in cystic fibrosis and control red blood cells. The 2,3-diphosphoglycerate content of the investigated cystic fibrosis red blood cells is normal.