CFTR HEK293 Recombinant Cell Line

Catalog #
60506
$7,500 *
Size: 2 vials
Qty
*US Pricing only. For international pricing, please contact your local distributor.
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Description

The CFTR HEK293 Cell Line expresses full length, wild-type human cystic fibrosis transmembrane conductance regulator (CFTR) protein (Genbank #P13569, NP_000483.3), with a C-terminal Streptavidin-Binding Peptide (SBP) tag.

Expression must be induced ≥24 hours prior to an experiment using 1 µg/ml Doxycycline and 3 mM Na-butyrate. The inducible expression of CFTR was confirmed by Western blotting and flow cytometry.

Purchase of this cell line is for research purposes only; commercial use requires a separate license. View the full terms and conditions.

Synonyms
Cystic fibrosis transmembrane conductance regulator, ATP-binding cassette sub-family C member 7, Channel conductance-controlling ATPase, cAMP-dependent chloride channel, ABCC7
Product Info
Storage and Usage
Citations
Host Cell Line
293HEK-Trex, Human Embryonic Kidney, epithelial-like cells, adherent
Species
Human
Supplied As
Each vial contains 2 x 106 cells in 1 ml of cell freezing medium (BPS Bioscience #79796)
Materials Required But Not Supplied

Materials Required for Cell Culture

Name Ordering Information
Thaw Medium 4 BPS Bioscience #60181
Growth Medium 4A BPS Bioscience #79535


Materials Required for Induction of CFTR Protein Expression

Name Ordering Information
Growth Medium 4C BPS Bioscience #79631
Genbank #
P13569
UniProt #
P13569
Mycoplasma Testing

The cell line has been screened to confirm the absence of Mycoplasma species.

Background

Cystic fibrosis transmembrane conductance regulator (CFTR) is a protein that in humans is encoded by the CFTR gene. CFTR is an ABC transporter-class ion channel that transports chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affect functioning of the chloride ion channels in these cell membranes, leading to cystic fibrosis. It is characterized by the triad of chronic bronchopulmonary disease (associated with recurrent respiratory infections), pancreatic insufficiency, which leads to malabsorption and growth retardation, and elevated sweat electrolytes.

References
1. Gadsby, D.C., et al. Nature 440 (7083): 477–483 (2006).
2. Hillier, L.W., et al. Nature 424:157-164 (2003).
3. McCann, C. M., et al. BioTechniques 38 (6):945–952 (2005).