<p>ND, not determined; VLPs do not encode an expressed transgene to allow titer determination.</p>a<p>Pseudotyped virus particles or VLPs were pelleted through sucrose and resuspended in 0.01 volumes of the original culture volume. A total of 0.2 ml of virus was used per assay with 10<sup>6</sup> cells and values were measured after 3 h of incubation.</p>b<p>Virus was prepared as above and used to infect HEK293-mCAT-1 cells. Titer was determined by limiting dilution using GFP reporter expression to count infected cells. Values for titer and entry assay are the mean±SD of 3 independent experiments.</p
<p>293T (left), CHO-K1 (right), and pgsA-745 (bottom) cells were seeded in 384-well plates and trans...
<p>(A) A549, MDCK and 293T cells were transduced with vectors encoding IFITM1, 2 or 3 or <i>cat</i> ...
<p>(A) Luciferase reporter constructs with different inserts were transiently transfected in HEK293 ...
<p>(A) The luciferase entry assay was performed using EVP (open bars) or VSVP (solid bars) or ZEBO-V...
a<p>NP2/CD4/CXCR4/CCR5 cells (1.5×10<sup>4</sup>) were infected with pseudotyped virus (50 ng p24Ag)...
<p>(A) 3X10<sup>5</sup> CEM-SS cells were infected with viral titers equivalent to 5 ng of p24 of VS...
<p>(A) Quantification of luciferase (Luc) expression from the pNL-Luc-E<sup>−</sup>R<sup>+</sup> (HI...
<p>HIV-Luc vector was co-transfected into 293 T cells with HN and F or VSV-G. Pseudoviruses were har...
<p>293T cells were transiently transfected with an infectious MoMLV or chimera proviral genome toget...
<p>EpoNi/22.1 cells incubated for 3 h in the absence (black bars) or presence (white bars) of ammoni...
<p>Coreceptor usage of the recombinant luciferase-reporter HIV was determined using NP2/CD4 cells ex...
<p>HEK 293T cells supernatant of newly generated stHIV with Env375H or Env 375Y viruses were infecte...
<p>(A) Minigenome assay. Different cell lines were transfected with all of the plasmids necessary fo...
<p>(A) VSV-G replication assay. Serial dilutions of pseudotyped virus (VSV-G envelope) were used in ...
<p>A panel of mutant and wild-type HN and F combinations were co-transfected into 293 T cells with t...
<p>293T (left), CHO-K1 (right), and pgsA-745 (bottom) cells were seeded in 384-well plates and trans...
<p>(A) A549, MDCK and 293T cells were transduced with vectors encoding IFITM1, 2 or 3 or <i>cat</i> ...
<p>(A) Luciferase reporter constructs with different inserts were transiently transfected in HEK293 ...
<p>(A) The luciferase entry assay was performed using EVP (open bars) or VSVP (solid bars) or ZEBO-V...
a<p>NP2/CD4/CXCR4/CCR5 cells (1.5×10<sup>4</sup>) were infected with pseudotyped virus (50 ng p24Ag)...
<p>(A) 3X10<sup>5</sup> CEM-SS cells were infected with viral titers equivalent to 5 ng of p24 of VS...
<p>(A) Quantification of luciferase (Luc) expression from the pNL-Luc-E<sup>−</sup>R<sup>+</sup> (HI...
<p>HIV-Luc vector was co-transfected into 293 T cells with HN and F or VSV-G. Pseudoviruses were har...
<p>293T cells were transiently transfected with an infectious MoMLV or chimera proviral genome toget...
<p>EpoNi/22.1 cells incubated for 3 h in the absence (black bars) or presence (white bars) of ammoni...
<p>Coreceptor usage of the recombinant luciferase-reporter HIV was determined using NP2/CD4 cells ex...
<p>HEK 293T cells supernatant of newly generated stHIV with Env375H or Env 375Y viruses were infecte...
<p>(A) Minigenome assay. Different cell lines were transfected with all of the plasmids necessary fo...
<p>(A) VSV-G replication assay. Serial dilutions of pseudotyped virus (VSV-G envelope) were used in ...
<p>A panel of mutant and wild-type HN and F combinations were co-transfected into 293 T cells with t...
<p>293T (left), CHO-K1 (right), and pgsA-745 (bottom) cells were seeded in 384-well plates and trans...
<p>(A) A549, MDCK and 293T cells were transduced with vectors encoding IFITM1, 2 or 3 or <i>cat</i> ...
<p>(A) Luciferase reporter constructs with different inserts were transiently transfected in HEK293 ...