<p>Late endosomes from BHK cells were submitted to solubilization in 1% Triton X-100 either at 4°C or at 37°C. The lysat was subsequently analyzed on an Optiprep gradient and 6 fractions were collected from the top. The total of each fraction was submitted to SDS-PAGE and Western blotting to detect flotillin-1 or to an aerolysin overlay to reveal GPI-anchored proteins.</p
The majority of glycosylphosphatidylinositol (GPI)-anchored proteins enter mammalian cells via the c...
<p>A. Negative-stain EM with Folch liposomes. Assays with endophilin-A1 (full-length or N-BAR domain...
In this paper, we studied the fate of endocytosed glycosylphosphatidyl inositol anchored proteins (G...
<p>Late endosomes were prepared from BHK cells using a sucrose step gradient, treated or not with ei...
<p>Late endosomes were purified from BHK cells and submitted to sub-organellar fractionation after b...
<p>A: DRMs were prepared from late endosomes (BHK cells +/− U18666A) by flotation on an OptiPrep gra...
Lysosomes are well-established as the main cellular organelles for the degradation of macromolecules...
Lysosomes are well-established as the main cellular organelles for the degradation of macromolecules...
<p>DRMs were prepared from late endosomes (BHK cells +/− U18666A) by flotation on an OptiPrep gradie...
<p>BHK cells were treated or not with U18666A at 3 µg/ml for 18 hours. A: Cells were labeled with fi...
and late endosomes and perhaps lysosomes, succes-sively acquiring markers of endosomal compartments ...
<p>Late endosomes were prepared from BHK cells, submitted to Triton X-100 solubilization and Optipre...
<p><b>A</b>. Following AP exposure to Caco-2BBe cells, GFP-labeled flagellin (green) was internalize...
<p><b>A. </b><i>Upper panel</i>, Immunoprecipitation (IP) of L1 from vesicle fractions was performed...
Previous studies provide evidence for an endocytic mechanism in mammalian cells that is distinct fro...
The majority of glycosylphosphatidylinositol (GPI)-anchored proteins enter mammalian cells via the c...
<p>A. Negative-stain EM with Folch liposomes. Assays with endophilin-A1 (full-length or N-BAR domain...
In this paper, we studied the fate of endocytosed glycosylphosphatidyl inositol anchored proteins (G...
<p>Late endosomes were prepared from BHK cells using a sucrose step gradient, treated or not with ei...
<p>Late endosomes were purified from BHK cells and submitted to sub-organellar fractionation after b...
<p>A: DRMs were prepared from late endosomes (BHK cells +/− U18666A) by flotation on an OptiPrep gra...
Lysosomes are well-established as the main cellular organelles for the degradation of macromolecules...
Lysosomes are well-established as the main cellular organelles for the degradation of macromolecules...
<p>DRMs were prepared from late endosomes (BHK cells +/− U18666A) by flotation on an OptiPrep gradie...
<p>BHK cells were treated or not with U18666A at 3 µg/ml for 18 hours. A: Cells were labeled with fi...
and late endosomes and perhaps lysosomes, succes-sively acquiring markers of endosomal compartments ...
<p>Late endosomes were prepared from BHK cells, submitted to Triton X-100 solubilization and Optipre...
<p><b>A</b>. Following AP exposure to Caco-2BBe cells, GFP-labeled flagellin (green) was internalize...
<p><b>A. </b><i>Upper panel</i>, Immunoprecipitation (IP) of L1 from vesicle fractions was performed...
Previous studies provide evidence for an endocytic mechanism in mammalian cells that is distinct fro...
The majority of glycosylphosphatidylinositol (GPI)-anchored proteins enter mammalian cells via the c...
<p>A. Negative-stain EM with Folch liposomes. Assays with endophilin-A1 (full-length or N-BAR domain...
In this paper, we studied the fate of endocytosed glycosylphosphatidyl inositol anchored proteins (G...