<p>(A) 293T cells were transfected with various GFP-Tat plasmids or the empty vector, and the fluorescence of GFP was examined by fluorescence microscopy 24 hours after transfection. (B) Experiments were performed as in panel A, and the expression levels of the GFP fusion proteins were measured via the ImageJ software and normalized to the vector group. WT, wild-type; ND, not determined.</p
<p>Native gel electrophoresis (3–12% gel) and subsequent western blotting of cleared lysates. UT; Un...
<p>(A) 293T cells were transfected with various GFP-Tat plasmids or the empty vector for 48 hours, a...
<p>Denaturing gel electrophoresis (4–12%) and subsequent western blotting of cleared lysates. UT; Un...
<p>(A) 293T cells were transfected with different GFP-Tat plasmids or the empty vector, and the subc...
<p>(A) 293T cells were transfected with different GFP-Tat plasmids or the empty vector. Cell extract...
<p>293T cells were transfected with an HIV-1 LTR-driven luciferase plasmid, a β-galactosidase-expres...
<p>293T cells were transfected with different GFP-Tat plasmids or the empty vector. Anti-GFP immunop...
<p>HEK293T cells were transiently co-transfected with SIVmac239 Env mutants and a GFP expression pla...
<p>The 293T cells were transfected by wild type (A) PRV gB or mutants (B-F) expression vectors to al...
<p>G∶C and A∶T focused mutations were monitored using <i>p</i>mutEGFP-TAG182, <i>p</i>mutEGFP-TAG52 ...
CHO cells were transfected with plasmids for each SOD1:YFP variant and representative pictures of di...
<p>(A) An LTR-GFP clone was exposed to varying amounts of purified Tat protein and analyzed by flow ...
<p>(<b>a</b>) 293 T cells were transfected with myc fusion constructs of wild type B Tat, C Tat and ...
<p>(A & B) HT1080 cells were transfected with control siRNA (Lanes 1) or DDX6 siRNA (Lanes 2 to 6) f...
<div><p>(A) FLP/MARCM system used to generate GFP-labeled homozygous mutant tracheal cell clones in ...
<p>Native gel electrophoresis (3–12% gel) and subsequent western blotting of cleared lysates. UT; Un...
<p>(A) 293T cells were transfected with various GFP-Tat plasmids or the empty vector for 48 hours, a...
<p>Denaturing gel electrophoresis (4–12%) and subsequent western blotting of cleared lysates. UT; Un...
<p>(A) 293T cells were transfected with different GFP-Tat plasmids or the empty vector, and the subc...
<p>(A) 293T cells were transfected with different GFP-Tat plasmids or the empty vector. Cell extract...
<p>293T cells were transfected with an HIV-1 LTR-driven luciferase plasmid, a β-galactosidase-expres...
<p>293T cells were transfected with different GFP-Tat plasmids or the empty vector. Anti-GFP immunop...
<p>HEK293T cells were transiently co-transfected with SIVmac239 Env mutants and a GFP expression pla...
<p>The 293T cells were transfected by wild type (A) PRV gB or mutants (B-F) expression vectors to al...
<p>G∶C and A∶T focused mutations were monitored using <i>p</i>mutEGFP-TAG182, <i>p</i>mutEGFP-TAG52 ...
CHO cells were transfected with plasmids for each SOD1:YFP variant and representative pictures of di...
<p>(A) An LTR-GFP clone was exposed to varying amounts of purified Tat protein and analyzed by flow ...
<p>(<b>a</b>) 293 T cells were transfected with myc fusion constructs of wild type B Tat, C Tat and ...
<p>(A & B) HT1080 cells were transfected with control siRNA (Lanes 1) or DDX6 siRNA (Lanes 2 to 6) f...
<div><p>(A) FLP/MARCM system used to generate GFP-labeled homozygous mutant tracheal cell clones in ...
<p>Native gel electrophoresis (3–12% gel) and subsequent western blotting of cleared lysates. UT; Un...
<p>(A) 293T cells were transfected with various GFP-Tat plasmids or the empty vector for 48 hours, a...
<p>Denaturing gel electrophoresis (4–12%) and subsequent western blotting of cleared lysates. UT; Un...