<p>Membranes were probed with organelle specific antibodies. A) Plasma membrane marker: Actin (C-11), 45 kDa; Golgi marker: 58 K Goli protein; endoplasmic reticulum marker: Calnexin, 90 kDa, and in B) Mitochondrial membrane marker: Cox1 (1D6), 39 kDa. Although mitochondrial membranes were present in the homogenate (step 1) these membranes were removed through the purification procedure we used to obtain RER membranes (step 4). Steps 1 and 4 are described in the “methods and materials” section.</p
<p>Equal amounts of protein (10 μg) were subjected to SDS/PAGE, immunoblotting and densitometric sca...
This study was aimed at preparing and characterizing plasma membranes (PM) from Chinese Hamster Ovar...
The Golgi membranes labeled with cis-Golgi marker GFP-SYP31 were isolated from suspension-cultured c...
A bulk fraction enriched with respect to neuronal cell bodies was used as starting material for the ...
<p>This figure illustrates results from cell compartment fractionation experiments yielding plasma-m...
Fractions enriched in Golgi membranes were prepared from rat liver by sucrose gradient ultracentrifu...
Fractions enriched in Golgi membranes were prepared from rat liver by sucrose gradient ultracentrifu...
<p>(A) Specificity of antibodies used to detect TOM20, Na<sup>+</sup>/K<sup>+</sup> ATPase α subunit...
<p><b>A</b>: In order to test the capacity of the purified recombinant fusion proteins to reincorpor...
Subcellular localization is crucial for the proper functioning of a protein. Deregulation of subcell...
<p>Molecular weight (kDa) of membrane markers is shown in parenthesis. GAPDH: Glyceraldehyde 3-phosp...
<p>(A) Percoll gradient biochemical fractionation scheme. (B) Electron micrograph of Huh7.5 cells. M...
The hypothesis that the Golgi apparatus is capable of sorting proteins and sending them to the plasm...
<p>(A): Stability of membrane and nuclear PrP<sup>c</sup> was analyzed by western blot after treatme...
<p>(A) Shown are representative fluorescent images from TIRF microscopy of CHO cells expressing the ...
<p>Equal amounts of protein (10 μg) were subjected to SDS/PAGE, immunoblotting and densitometric sca...
This study was aimed at preparing and characterizing plasma membranes (PM) from Chinese Hamster Ovar...
The Golgi membranes labeled with cis-Golgi marker GFP-SYP31 were isolated from suspension-cultured c...
A bulk fraction enriched with respect to neuronal cell bodies was used as starting material for the ...
<p>This figure illustrates results from cell compartment fractionation experiments yielding plasma-m...
Fractions enriched in Golgi membranes were prepared from rat liver by sucrose gradient ultracentrifu...
Fractions enriched in Golgi membranes were prepared from rat liver by sucrose gradient ultracentrifu...
<p>(A) Specificity of antibodies used to detect TOM20, Na<sup>+</sup>/K<sup>+</sup> ATPase α subunit...
<p><b>A</b>: In order to test the capacity of the purified recombinant fusion proteins to reincorpor...
Subcellular localization is crucial for the proper functioning of a protein. Deregulation of subcell...
<p>Molecular weight (kDa) of membrane markers is shown in parenthesis. GAPDH: Glyceraldehyde 3-phosp...
<p>(A) Percoll gradient biochemical fractionation scheme. (B) Electron micrograph of Huh7.5 cells. M...
The hypothesis that the Golgi apparatus is capable of sorting proteins and sending them to the plasm...
<p>(A): Stability of membrane and nuclear PrP<sup>c</sup> was analyzed by western blot after treatme...
<p>(A) Shown are representative fluorescent images from TIRF microscopy of CHO cells expressing the ...
<p>Equal amounts of protein (10 μg) were subjected to SDS/PAGE, immunoblotting and densitometric sca...
This study was aimed at preparing and characterizing plasma membranes (PM) from Chinese Hamster Ovar...
The Golgi membranes labeled with cis-Golgi marker GFP-SYP31 were isolated from suspension-cultured c...