<p>Calumenin or CFTR (green) in CFBE41o- wild-type or F508del cells were visualized using fluorescence microscopy. Second labeling was performed for either PDI (an ER marker). Golgi marker or EEA1 (marker for endosomal vesicles) (red). The nuclei were stained blue with DAPI. Colocalisation of green and red pixels was detected in merged images (yellow). <b>A.</b> Calumenin and PDI (for ER staining) <b>B.</b> Calumenin and Golgi and <b>C.</b> Calumenin and EEA1 in CFBE41o- cells expressing F508del-CFTR. <b>D.</b> CFTR and EEA1 in CFBE41o- cells expressing F508del-CFTR. Scale bar: 20 µm.</p
<p>A) Western blot analysis of CFTR expression in NU12 and HU33 cells transiently transfected with t...
Cystic Fibrosis (CF) is characterized by mutations in the CFTR gene that encodes for an apical plasm...
<p><b>A</b> SCC-13 cells were infected by 10 MOI tAd5-EV or tAd5-TIG3 and after 24 h fixed and stain...
<p>Calumenin or CFTR (green) in CFBE41o- wild-type or F508del cells were visualized using fluorescen...
Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian populati...
Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian populati...
<p><b>A,</b> Example of detection of calumenin in Wt-CFTR and G551D expressing cells, assessed by we...
<p>The N terminus of CFTR was tagged with YFP, and CFP was tagged to the C terminus of CAL was tagge...
International audienceCystic Fibrosis (CF) is the most frequent fatal genetic disease in Caucasian p...
<p>(A) HeLa cells stably expressing wt-CFTR were transiently transfected with an empty COMMD1 vector...
<p>Expression of Fra-1 (upper left columns), c-Fos (lower left columns) and the ER marker calnexin (...
<p>A) Cell images from a FRAP experiment: YFP-CFTR signal in a HEK293 T cell over-expressing CFP-WT ...
The cystic fibrosis transmembrane regulator (CFTR) is a cyclic-AMP dependent chloride channel expres...
<div><p>The cystic fibrosis transmembrane regulator (CFTR) is a cyclic-AMP dependent chloride channe...
La mucoviscidose (Cystic Fibrosis, CF) est caractérisée par des mutations dans le gène CFTR codant p...
<p>A) Western blot analysis of CFTR expression in NU12 and HU33 cells transiently transfected with t...
Cystic Fibrosis (CF) is characterized by mutations in the CFTR gene that encodes for an apical plasm...
<p><b>A</b> SCC-13 cells were infected by 10 MOI tAd5-EV or tAd5-TIG3 and after 24 h fixed and stain...
<p>Calumenin or CFTR (green) in CFBE41o- wild-type or F508del cells were visualized using fluorescen...
Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian populati...
Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the Caucasian populati...
<p><b>A,</b> Example of detection of calumenin in Wt-CFTR and G551D expressing cells, assessed by we...
<p>The N terminus of CFTR was tagged with YFP, and CFP was tagged to the C terminus of CAL was tagge...
International audienceCystic Fibrosis (CF) is the most frequent fatal genetic disease in Caucasian p...
<p>(A) HeLa cells stably expressing wt-CFTR were transiently transfected with an empty COMMD1 vector...
<p>Expression of Fra-1 (upper left columns), c-Fos (lower left columns) and the ER marker calnexin (...
<p>A) Cell images from a FRAP experiment: YFP-CFTR signal in a HEK293 T cell over-expressing CFP-WT ...
The cystic fibrosis transmembrane regulator (CFTR) is a cyclic-AMP dependent chloride channel expres...
<div><p>The cystic fibrosis transmembrane regulator (CFTR) is a cyclic-AMP dependent chloride channe...
La mucoviscidose (Cystic Fibrosis, CF) est caractérisée par des mutations dans le gène CFTR codant p...
<p>A) Western blot analysis of CFTR expression in NU12 and HU33 cells transiently transfected with t...
Cystic Fibrosis (CF) is characterized by mutations in the CFTR gene that encodes for an apical plasm...
<p><b>A</b> SCC-13 cells were infected by 10 MOI tAd5-EV or tAd5-TIG3 and after 24 h fixed and stain...