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ly6e antibodies for mouse  (Novus Biologicals)


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    Novus Biologicals ly6e antibodies for mouse
    Ly6e Antibodies For Mouse, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ly6e antibodies for mouse/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
    ly6e antibodies for mouse - by Bioz Stars, 2026-05
    90/100 stars

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    Novus Biologicals ly6e antibodies for mouse
    Ly6e Antibodies For Mouse, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ly6e antibodies for mouse/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
    ly6e antibodies for mouse - by Bioz Stars, 2026-05
    90/100 stars
      Buy from Supplier

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    Genentech inc mouse anti-ly6e monoclonal antibody 4d8.6.7
    a The expression levels of <t>LY6E</t> . Each symbol indicates the result from one replicate, and the bars with error bars indicate the averages with SEMs of three independent replicates. RPKM, reads per kilobase of exon per million mapped reads. b,c Effect of LY6E overexpression on cell-free HIV-1 infection. b Western blotting. Parental Jurkat-CCR5 cells (’Parent’), empty vector-transduced cells (Empty), and LY6E-HA-transduced cells (’LY6E-HA’) were prepared as described in Methods, and the LY6E-HA expression is detected by Western blotting. A representative result is shown. Alpha-tubulin (TUBA) is used as an internal control. c Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, and 6 ml) corresponds to that shown in . Single round infection assay was performed at four different cell-virus densities. d,e Effect of LY6E KO on cell-free HIV-1 infection. d Western blotting. Parental Jurkat-CCR5 cells (’Parent’), non-target sgRNA-transduced cells (’SgNT’), and LY6E KO cells ( ’LY6E KO’) were prepared as described in Materials and Methods, and endogenous LY6E expression is detected by Western blotting. A representative result is shown. TUBA is used as an internal control. e Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, 3 and 6 ml) corresponds to that shown in . Single round infection assay was performed at five different cell-virus densities. In panels c and e , each dot indicates the result from one culture, and three independent experiments were performed. The bars with error bars are the averages and SEMs of three independent experiments. Asterisks indicate statistically significant differences determined by Student’s t test ( p <0.05).
    Mouse Anti Ly6e Monoclonal Antibody 4d8.6.7, supplied by Genentech inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti-ly6e monoclonal antibody 4d8.6.7/product/Genentech inc
    Average 90 stars, based on 1 article reviews
    mouse anti-ly6e monoclonal antibody 4d8.6.7 - by Bioz Stars, 2026-05
    90/100 stars
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    a The expression levels of LY6E . Each symbol indicates the result from one replicate, and the bars with error bars indicate the averages with SEMs of three independent replicates. RPKM, reads per kilobase of exon per million mapped reads. b,c Effect of LY6E overexpression on cell-free HIV-1 infection. b Western blotting. Parental Jurkat-CCR5 cells (’Parent’), empty vector-transduced cells (Empty), and LY6E-HA-transduced cells (’LY6E-HA’) were prepared as described in Methods, and the LY6E-HA expression is detected by Western blotting. A representative result is shown. Alpha-tubulin (TUBA) is used as an internal control. c Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, and 6 ml) corresponds to that shown in . Single round infection assay was performed at four different cell-virus densities. d,e Effect of LY6E KO on cell-free HIV-1 infection. d Western blotting. Parental Jurkat-CCR5 cells (’Parent’), non-target sgRNA-transduced cells (’SgNT’), and LY6E KO cells ( ’LY6E KO’) were prepared as described in Materials and Methods, and endogenous LY6E expression is detected by Western blotting. A representative result is shown. TUBA is used as an internal control. e Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, 3 and 6 ml) corresponds to that shown in . Single round infection assay was performed at five different cell-virus densities. In panels c and e , each dot indicates the result from one culture, and three independent experiments were performed. The bars with error bars are the averages and SEMs of three independent experiments. Asterisks indicate statistically significant differences determined by Student’s t test ( p <0.05).

    Journal: PLoS Computational Biology

    Article Title: Antithetic effect of interferon-α on cell-free and cell-to-cell HIV-1 infection

    doi: 10.1371/journal.pcbi.1010053

    Figure Lengend Snippet: a The expression levels of LY6E . Each symbol indicates the result from one replicate, and the bars with error bars indicate the averages with SEMs of three independent replicates. RPKM, reads per kilobase of exon per million mapped reads. b,c Effect of LY6E overexpression on cell-free HIV-1 infection. b Western blotting. Parental Jurkat-CCR5 cells (’Parent’), empty vector-transduced cells (Empty), and LY6E-HA-transduced cells (’LY6E-HA’) were prepared as described in Methods, and the LY6E-HA expression is detected by Western blotting. A representative result is shown. Alpha-tubulin (TUBA) is used as an internal control. c Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, and 6 ml) corresponds to that shown in . Single round infection assay was performed at four different cell-virus densities. d,e Effect of LY6E KO on cell-free HIV-1 infection. d Western blotting. Parental Jurkat-CCR5 cells (’Parent’), non-target sgRNA-transduced cells (’SgNT’), and LY6E KO cells ( ’LY6E KO’) were prepared as described in Materials and Methods, and endogenous LY6E expression is detected by Western blotting. A representative result is shown. TUBA is used as an internal control. e Single-round infection assay under different density conditions. The V/C at different five culture conditions (0.5, 1, 2, 3 and 6 ml) corresponds to that shown in . Single round infection assay was performed at five different cell-virus densities. In panels c and e , each dot indicates the result from one culture, and three independent experiments were performed. The bars with error bars are the averages and SEMs of three independent experiments. Asterisks indicate statistically significant differences determined by Student’s t test ( p <0.05).

    Article Snippet: LY6E was detected using a mouse anti-LY6E monoclonal antibody (4D8.6.7, Genentech), and beta-actin (ACTB) was detected using peroxidase-conjugated anti-ACTB monoclonal antibody (AC-15, Sigma).

    Techniques: Expressing, Over Expression, Infection, Western Blot, Plasmid Preparation, Control, Virus