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the empty pgl3 basic vector was used as the negative control  (Promega)

 
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    Structured Review

    Promega the empty pgl3 basic vector was used as the negative control
    Dual-luciferase reporter assay in the 293T cell line. The <t>pGL3-Basic</t> and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.
    The Empty Pgl3 Basic Vector Was Used As The Negative Control, supplied by Promega, 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/the empty pgl3 basic vector was used as the negative control/product/Promega
    Average 90 stars, based on 1 article reviews
    the empty pgl3 basic vector was used as the negative control - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "Significant association of EED promoter hypomethylation with colorectal cancer"

    Article Title: Significant association of EED promoter hypomethylation with colorectal cancer

    Journal: Oncology Letters

    doi: 10.3892/ol.2019.10432

    Dual-luciferase reporter assay in the 293T cell line. The pGL3-Basic and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.
    Figure Legend Snippet: Dual-luciferase reporter assay in the 293T cell line. The pGL3-Basic and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.

    Techniques Used: Luciferase, Reporter Assay, Recombinant, Plasmid Preparation



    Similar Products

    90
    Promega the empty pgl3 basic vector was used as the negative control
    Dual-luciferase reporter assay in the 293T cell line. The <t>pGL3-Basic</t> and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.
    The Empty Pgl3 Basic Vector Was Used As The Negative Control, supplied by Promega, 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/the empty pgl3 basic vector was used as the negative control/product/Promega
    Average 90 stars, based on 1 article reviews
    the empty pgl3 basic vector was used as the negative control - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    90
    Promega the empty pgl3-basic vector was used as negative control
    Dual-luciferase reporter assay in HEK-293T cell line. The <t>pGL3</t> Basic and promoter vectors were used as negative and positive control in this study, respectively. Relative luciferase activity was performed in triplicates.
    The Empty Pgl3 Basic Vector Was Used As Negative Control, supplied by Promega, 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/the empty pgl3-basic vector was used as negative control/product/Promega
    Average 90 stars, based on 1 article reviews
    the empty pgl3-basic vector was used as negative control - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    Image Search Results


    Dual-luciferase reporter assay in the 293T cell line. The pGL3-Basic and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.

    Journal: Oncology Letters

    Article Title: Significant association of EED promoter hypomethylation with colorectal cancer

    doi: 10.3892/ol.2019.10432

    Figure Lengend Snippet: Dual-luciferase reporter assay in the 293T cell line. The pGL3-Basic and pGL3-Promoter vectors were used as negative and positive controls, respectively. The relative luciferase level is displayed for pGL3-Promoter, pGL3-Basic and pGL3-EED The pGL3-EED indicates the recombinant EED fragment ligated to the pGL3-Basic vector. An analysis of variance and Bonferroni's correction were applied for statistical analysis. P<0.05 was considered to indicate a statistically significant difference. *P<0.0001. EED, embryonic ectoderm development; Luc, luciferase.

    Article Snippet: The empty pGL3 basic vector was used as the negative control and the pGL3 promoter vector (both Promega Cooperation, Madison, WI, USA) was used as the positive control, which contained an SV40 promoter upstream of the luciferase gene.

    Techniques: Luciferase, Reporter Assay, Recombinant, Plasmid Preparation

    Dual-luciferase reporter assay in HEK-293T cell line. The pGL3 Basic and promoter vectors were used as negative and positive control in this study, respectively. Relative luciferase activity was performed in triplicates.

    Journal: Scientific Reports

    Article Title: Elevated UMOD methylation level in peripheral blood is associated with gout risk

    doi: 10.1038/s41598-017-11627-w

    Figure Lengend Snippet: Dual-luciferase reporter assay in HEK-293T cell line. The pGL3 Basic and promoter vectors were used as negative and positive control in this study, respectively. Relative luciferase activity was performed in triplicates.

    Article Snippet: The empty pGL3-Basic vector was used as negative control, and the pGL3-Control vector, (Promega, Madison city, WI, USA) containing an SV40 promoter upstream of the luciferase gene was used as positive control.

    Techniques: Luciferase, Reporter Assay, Positive Control, Activity Assay