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ifn β promoter luciferase reporter  (Addgene inc)


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    Structured Review

    Addgene inc ifn β promoter luciferase reporter
    Ifn β Promoter Luciferase Reporter, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ifn+%CE%B2+promoter+luciferase+reporter/IFN-Beta_pGL3+(Plasmid+%23102597)/pm39404379-79-14-19
    Average 94 stars, based on 62 article reviews
    ifn β promoter luciferase reporter - by Bioz Stars, 2026-09
    94/100 stars

    Images

    Related Articles

    Luciferase:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: Fluorescent blot detection was performed using an Odyssey ® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonE-driven Photinus [ ], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: Fluorescent blot detection was performed using an Odyssey® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonEdriven Photinus [15], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: Identification of a Papain-Like Protease Inhibitor with Potential for Repurposing in Combination with an Mpro Protease Inhibitor for Treatment of SARS-CoV-2
    Article Snippet: .. An Addgene plasmid was used for the IFN-β promoter luciferase reporter (IFNBeta_pGL3, #102597). .. To make the NF-κB signaling reporter, a gene block containing 5 tandem consensus NF-κB binding sites (Badr et al 2009; Ngo et al 2020), followed by the -55 to +19 region of the human IFN-β gene (UCSC Genome Browser) was synthesized by Integrated DNA Technologies (Alvarez and Yao, unpublished).

    Article Title: Identification of a Papain-Like Protease Inhibitor with Potential for Repurposing in Combination with an M pro Protease Inhibitor for Treatment of SARS-CoV-2
    Article Snippet: .. An Addgene plasmid was used for the IFN-β promoter luciferase reporter (IFN-Beta_pGL3, #102597). .. To make the NF-κB signaling reporter, a gene block containing 5 tandem consensus NF-κB binding sites (Badr et al 2009; Ngo et al 2020), followed by the -55 to +19 region of the human IFN-β gene (UCSC Genome Browser) was synthesized by Integrated DNA Technologies (Alvarez and Yao, unpublished).

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: The plasmid encoding the N-terminal fragment of TonEBP generated by SARS-CoV-2 NSP5 cleavage was cloned into the pCMV-tag 2B vector (#211172, Agilent Technologies, Santa Clara, CA, USA) by amplification and standard restriction cloning. .. The IFN-β promoter luciferase reporter (#102597), as well as transient expression vectors for MDA5 (#52876), MAVS (#52135), TBK1 (#131792), IRF3 (#127663), and p65 (#111192), were obtained from Addgene. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: The plasmid encoding the N-terminal fragment of TonEBP generated by SARS-CoV-2 NSP5 cleavage was cloned into the pCMV-tag 2B vector (#211172, Agilent Technologies, Santa Clara, CA, USA) by amplification and standard restriction cloning. .. The IFN-β promoter luciferase reporter (#102597), as well as transient expression vectors for MDA5 (#52876), MAVS (#52135), TBK1 (#131792), IRF3 (#127663), and p65 (#111192), were obtained from Addgene. ..

    Construct:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: Fluorescent blot detection was performed using an Odyssey ® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonE-driven Photinus [ ], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: Fluorescent blot detection was performed using an Odyssey® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonEdriven Photinus [15], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Plasmid Preparation:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: Fluorescent blot detection was performed using an Odyssey ® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonE-driven Photinus [ ], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: Fluorescent blot detection was performed using an Odyssey® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonEdriven Photinus [15], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: Identification of a Papain-Like Protease Inhibitor with Potential for Repurposing in Combination with an Mpro Protease Inhibitor for Treatment of SARS-CoV-2
    Article Snippet: .. An Addgene plasmid was used for the IFN-β promoter luciferase reporter (IFNBeta_pGL3, #102597). .. To make the NF-κB signaling reporter, a gene block containing 5 tandem consensus NF-κB binding sites (Badr et al 2009; Ngo et al 2020), followed by the -55 to +19 region of the human IFN-β gene (UCSC Genome Browser) was synthesized by Integrated DNA Technologies (Alvarez and Yao, unpublished).

    Article Title: Identification of a Papain-Like Protease Inhibitor with Potential for Repurposing in Combination with an M pro Protease Inhibitor for Treatment of SARS-CoV-2
    Article Snippet: .. An Addgene plasmid was used for the IFN-β promoter luciferase reporter (IFN-Beta_pGL3, #102597). .. To make the NF-κB signaling reporter, a gene block containing 5 tandem consensus NF-κB binding sites (Badr et al 2009; Ngo et al 2020), followed by the -55 to +19 region of the human IFN-β gene (UCSC Genome Browser) was synthesized by Integrated DNA Technologies (Alvarez and Yao, unpublished).

    Control:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: Fluorescent blot detection was performed using an Odyssey ® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonE-driven Photinus [ ], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: Fluorescent blot detection was performed using an Odyssey® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonEdriven Photinus [15], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Transfection:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: Fluorescent blot detection was performed using an Odyssey ® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonE-driven Photinus [ ], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: Fluorescent blot detection was performed using an Odyssey® CLx Imaging System (LI-COR). .. HEK293T cells were co-transfected with the indicated luciferase constructs of TonEdriven Photinus [15], or IFN-β promoter luciferase reporter (#102597, Addgene) and the Renilla luciferase plasmid (pRL-TK), which was used as an internal control for transfection efficiency. ..

    Expressing:

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression
    Article Snippet: The plasmid encoding the N-terminal fragment of TonEBP generated by SARS-CoV-2 NSP5 cleavage was cloned into the pCMV-tag 2B vector (#211172, Agilent Technologies, Santa Clara, CA, USA) by amplification and standard restriction cloning. .. The IFN-β promoter luciferase reporter (#102597), as well as transient expression vectors for MDA5 (#52876), MAVS (#52135), TBK1 (#131792), IRF3 (#127663), and p65 (#111192), were obtained from Addgene. ..

    Article Title: A Gain-of-Function Cleavage of TonEBP by Coronavirus NSP5 to Suppress IFN-β Expression.
    Article Snippet: The plasmid encoding the N-terminal fragment of TonEBP generated by SARS-CoV-2 NSP5 cleavage was cloned into the pCMV-tag 2B vector (#211172, Agilent Technologies, Santa Clara, CA, USA) by amplification and standard restriction cloning. .. The IFN-β promoter luciferase reporter (#102597), as well as transient expression vectors for MDA5 (#52876), MAVS (#52135), TBK1 (#131792), IRF3 (#127663), and p65 (#111192), were obtained from Addgene. ..



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    Image Search Results


    The N terminus is necessary for SARS-CoV-2 Nsp1 to inhibit protein translation. (A) Schematic diagram of SARS-CoV-2 Nsp1 and its truncated forms. (B to D) HEK293T cells (5 × 10 4 cells/well, 48-well plates) were cotransfected with 50 ng firefly luciferase reporter plasmid for the IFN-β promoter (IFNβ-Luc), 5 ng Renilla luciferase reporter plasmid for herpes simplex virus thymidine kinase promoter (HSV-TK-Luc; used as an internal control), and 200 ng SARS-CoV-2 Nsp1 plasmid or its indicated truncated plasmid. SeV infection was performed at 24 h posttransfection. The reporter activity was detected with a dual-luciferase reporter system at 10 h postinfection (B and C). Total cellular RNA was extracted for mRNA analysis by real-time PCR (D). Data in panels B to D are means and standard errors of the means (SEM) from at least three independent experiments and were normalized to the control group. The P value was calculated in GraphPad Prism 8.2.1 using ordinary one-way analysis of variance (ANOVA) and subjected to multiple-testing correction by the false-discovery-rate (FDR) method. See also Fig. S2.

    Journal: Microbiology Spectrum

    Article Title: Structural Basis and Function of the N Terminus of SARS-CoV-2 Nonstructural Protein 1

    doi: 10.1128/Spectrum.00169-21

    Figure Lengend Snippet: The N terminus is necessary for SARS-CoV-2 Nsp1 to inhibit protein translation. (A) Schematic diagram of SARS-CoV-2 Nsp1 and its truncated forms. (B to D) HEK293T cells (5 × 10 4 cells/well, 48-well plates) were cotransfected with 50 ng firefly luciferase reporter plasmid for the IFN-β promoter (IFNβ-Luc), 5 ng Renilla luciferase reporter plasmid for herpes simplex virus thymidine kinase promoter (HSV-TK-Luc; used as an internal control), and 200 ng SARS-CoV-2 Nsp1 plasmid or its indicated truncated plasmid. SeV infection was performed at 24 h posttransfection. The reporter activity was detected with a dual-luciferase reporter system at 10 h postinfection (B and C). Total cellular RNA was extracted for mRNA analysis by real-time PCR (D). Data in panels B to D are means and standard errors of the means (SEM) from at least three independent experiments and were normalized to the control group. The P value was calculated in GraphPad Prism 8.2.1 using ordinary one-way analysis of variance (ANOVA) and subjected to multiple-testing correction by the false-discovery-rate (FDR) method. See also Fig. S2.

    Article Snippet: The IFN-β promoter–firefly luciferase reporter plasmid was purchased from Clone Tech (Somis, CA), and the herpes simplex virus thymidine kinase promoter– Renilla luciferase reporter plasmid (pRL-TK) was purchased from Promega (San Luis Obispo, CA).

    Techniques: Luciferase, Plasmid Preparation, Infection, Activity Assay, Real-time Polymerase Chain Reaction

    The N-terminal sequence of Nsp1 is not specific for translation inhibition. (A) The colocalization of EGFP and EGFP-fused Nsp1/126–180 (green) with ribosome (immunostained with anti-RPS6 antibody [red]) was analyzed by immunofluorescence in HEK293T cells. The intensity profile describes the distribution of EGFP or EGFP-fused Nsp1/126–180 and RPS6-specific fluorescence along the indicated line. (B) Pearson’s correlation between Nsp1 or its truncated mutants and RPS6 was analyzed and displayed. The P value was calculated in GraphPad Prism 8.2.1 using ordinary one-way ANOVA and subjected to multiple-testing correction by FDR method. (C to F) HEK293T cells (5 × 10 4 cells/well, 48-well plates) were cotransfected with 50 ng firefly luciferase reporter plasmid for IFN-β promoter (IFNβ-Luc), 5 ng Renilla luciferase reporter plasmid for the herpes simplex virus thymidine kinase promoter (HSV-TK-Luc; used as an internal control), and 200 ng of the indicated truncated plasmid or EGFP fusion-expressing plasmid. SeV infection was performed at 24 h posttransfection. The reporter activity was detected by dual-luciferase reporter system at 10 h postinfection. Data in panels C to F are means and SEM from at least three independent experiments and were normalized to the control group.

    Journal: Microbiology Spectrum

    Article Title: Structural Basis and Function of the N Terminus of SARS-CoV-2 Nonstructural Protein 1

    doi: 10.1128/Spectrum.00169-21

    Figure Lengend Snippet: The N-terminal sequence of Nsp1 is not specific for translation inhibition. (A) The colocalization of EGFP and EGFP-fused Nsp1/126–180 (green) with ribosome (immunostained with anti-RPS6 antibody [red]) was analyzed by immunofluorescence in HEK293T cells. The intensity profile describes the distribution of EGFP or EGFP-fused Nsp1/126–180 and RPS6-specific fluorescence along the indicated line. (B) Pearson’s correlation between Nsp1 or its truncated mutants and RPS6 was analyzed and displayed. The P value was calculated in GraphPad Prism 8.2.1 using ordinary one-way ANOVA and subjected to multiple-testing correction by FDR method. (C to F) HEK293T cells (5 × 10 4 cells/well, 48-well plates) were cotransfected with 50 ng firefly luciferase reporter plasmid for IFN-β promoter (IFNβ-Luc), 5 ng Renilla luciferase reporter plasmid for the herpes simplex virus thymidine kinase promoter (HSV-TK-Luc; used as an internal control), and 200 ng of the indicated truncated plasmid or EGFP fusion-expressing plasmid. SeV infection was performed at 24 h posttransfection. The reporter activity was detected by dual-luciferase reporter system at 10 h postinfection. Data in panels C to F are means and SEM from at least three independent experiments and were normalized to the control group.

    Article Snippet: The IFN-β promoter–firefly luciferase reporter plasmid was purchased from Clone Tech (Somis, CA), and the herpes simplex virus thymidine kinase promoter– Renilla luciferase reporter plasmid (pRL-TK) was purchased from Promega (San Luis Obispo, CA).

    Techniques: Sequencing, Inhibition, Immunofluorescence, Fluorescence, Luciferase, Plasmid Preparation, Expressing, Infection, Activity Assay