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scramble control sgrna  (Addgene inc)


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    Structured Review

    Addgene inc scramble control sgrna
    Scramble Control Sgrna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1044 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/scramble control sgrna/product/Addgene inc
    Average 96 stars, based on 1044 article reviews
    scramble control sgrna - by Bioz Stars, 2026-03
    96/100 stars

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    CTD serine 2, but not serine 7, is required for efficient viral gene expression. HEK-293T cells were co-transfected with a construct expressing a <t>sgRNA</t> transcribed by <t>Pol</t> <t>III</t> as a transfection control and plasmids expressing amanitin-resistant RPB1 with wild-type (WT) or indicated mutant CTDs, or the control vector pcDNA3 lacking any polymerase. The next day, α-amanitin was added to degrade endogenous RPB1 for 24 h followed by infection with HSV-1 strain 17+, and viral gene expression was measured by RT-qPCR at 24 hpi. Means of three biological replicates with standard error are plotted. Statistically significant differences to mock are indicated as * P < 0.05, ** P < 0.01, *** P < 0.001. S2A: serine 2 to alanine, S7A: serine 7 to alanine, S7E: serine 7 to glutamate.
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    CTD serine 2, but not serine 7, is required for efficient viral gene expression. HEK-293T cells were co-transfected with a construct expressing a <t>sgRNA</t> transcribed by <t>Pol</t> <t>III</t> as a transfection control and plasmids expressing amanitin-resistant RPB1 with wild-type (WT) or indicated mutant CTDs, or the control vector pcDNA3 lacking any polymerase. The next day, α-amanitin was added to degrade endogenous RPB1 for 24 h followed by infection with HSV-1 strain 17+, and viral gene expression was measured by RT-qPCR at 24 hpi. Means of three biological replicates with standard error are plotted. Statistically significant differences to mock are indicated as * P < 0.05, ** P < 0.01, *** P < 0.001. S2A: serine 2 to alanine, S7A: serine 7 to alanine, S7E: serine 7 to glutamate.
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    CTD serine 2, but not serine 7, is required for efficient viral gene expression. HEK-293T cells were co-transfected with a construct expressing a sgRNA transcribed by Pol III as a transfection control and plasmids expressing amanitin-resistant RPB1 with wild-type (WT) or indicated mutant CTDs, or the control vector pcDNA3 lacking any polymerase. The next day, α-amanitin was added to degrade endogenous RPB1 for 24 h followed by infection with HSV-1 strain 17+, and viral gene expression was measured by RT-qPCR at 24 hpi. Means of three biological replicates with standard error are plotted. Statistically significant differences to mock are indicated as * P < 0.05, ** P < 0.01, *** P < 0.001. S2A: serine 2 to alanine, S7A: serine 7 to alanine, S7E: serine 7 to glutamate.

    Journal: Journal of Virology

    Article Title: Herpes simplex virus 1 inhibits phosphorylation of RNA polymerase II CTD serine-7

    doi: 10.1128/jvi.01178-24

    Figure Lengend Snippet: CTD serine 2, but not serine 7, is required for efficient viral gene expression. HEK-293T cells were co-transfected with a construct expressing a sgRNA transcribed by Pol III as a transfection control and plasmids expressing amanitin-resistant RPB1 with wild-type (WT) or indicated mutant CTDs, or the control vector pcDNA3 lacking any polymerase. The next day, α-amanitin was added to degrade endogenous RPB1 for 24 h followed by infection with HSV-1 strain 17+, and viral gene expression was measured by RT-qPCR at 24 hpi. Means of three biological replicates with standard error are plotted. Statistically significant differences to mock are indicated as * P < 0.05, ** P < 0.01, *** P < 0.001. S2A: serine 2 to alanine, S7A: serine 7 to alanine, S7E: serine 7 to glutamate.

    Article Snippet: For qPCR analysis, the assay was repeated but scaled up to 24-well plates, this time using 50 ng of the vector pU6.scr_sgRNA in place of Azurite, which expresses a scrambled control sgRNA based on Addgene #62285 from the RNA Pol III promoter U6.

    Techniques: Gene Expression, Transfection, Construct, Expressing, Control, Mutagenesis, Plasmid Preparation, Infection, Quantitative RT-PCR