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plasmids pgl3 basic  (Addgene inc)


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    Structured Review

    Addgene inc plasmids pgl3 basic
    Plasmids Pgl3 Basic, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pgl3-basic+plasmid/pRF%2B275Dux4+(Plasmid+%2321293)/pmc12666318-90-3-5
    Average 93 stars, based on 29 article reviews
    plasmids pgl3 basic - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Sequencing:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Chromatin Immunoprecipitation:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Plasmid Preparation:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Article Title: Bone Metastatic Progression of Prostate Cancer is Regulated by TRIM28-LDHA Mediated Metabolism
    Article Snippet: LDHA promoter luciferase reporter assays were conducted according to the manual of Dual-Luciferase Reporter Assay System from Promega. .. Briefly, C4–2B cells were seeded in a 24-well plate and co-transfected with the Renilla expression plasmid pRL-TK (RRID:Addgene_27163) and the reporter constructs for LDHA promoter in pGL3 vector (RRID:Addgene_212937). ..

    Article Title: UHRF1 restricts HCoV-229E infection through epigenetic silencing of the viral receptor APN
    Article Snippet: A Chemiluminescent EMSA kit (Beyotime #GS009) was used to detect interactions between the probes and nuclear proteins extracted from control and UHRF1 -knockout A549 cells using NE-PERTM Nuclear and Cytoplasmic Extraction Reagents (Thermo #78833). .. The APN promoter sequences (−153 to −1) were cloned into the pGL3 Basic vector (Addgene ##212936), resulting in the plasmid pGL3-APN-Luc. .. The pGL3-APN-Luc plasmid was methylated in vitro using CpG Methyltransferase M.SssI (NEB #M0226S).

    Recombinant:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Software:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Imaging:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Light Microscopy:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Modification:

    Article Title: Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling.
    Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Metabolomics RAW data This paper NMDR: ST004216; DIO: https://doi.org/ 10.21228/M82V85 Experimental models: Cell lines C3H/10T1/2 Procell Life Science & Technology CL-0325 3T3-L1 National Collection of Autjenticated Cell Cultures GNM25 HUVEC Procell Life Science & Technology N/A 293T Procell Life Science & Technology CL-0005 Experimental models: Organisms/strains Mouse: C57BL/6 mice Charles River Laboratories N/A Mouse: OGT-flox and Adipoq-Cre mice Jackson Laboratory N/A Mouse: Ucp1-CreER mice Shanghai Model Organisms Center NM-KI-190102 Oligonucleotides siRNA targeting sequence: OGT: GAUUAAGCCUGUUGAAGUC Peng et al.54 N/A siRNA targeting sequence: SP1: CCAGCAACAUGGGAAUUAUdTdT Lu et al.55 N/A siRNA targeting sequence: KCP#1: CTTCACCCTCCAAGAGAAT This paper N/A siRNA targeting sequence: KCP#2: CAACCTATGCACCTGCCTT This paper N/A Real-time qPCR primers This paper See Table S1 ChIP-PCR primers This paper See Table S2 Plasmid construction primers This paper See Tables S3 and S4 Recombinant DNA pGL3 Basic Vector Addgene Cat# 212936 pcDNA3-Flag-SP1 Addgene Cat# 232649 Software and algorithms ImageJ National Institutes of Health https://imagej.net/ij/ ZEN Digital Imaging for Light Microscopy v 3.4 (blue edition) Zeiss https://www.zeiss.com/microscopy/en/ products/software/zeiss-zen-lite.html Graphpad Prism 8 Graphpad Software https://www.graphpad.com/features AngioTool – https://angiotool.software.informer.com/ PyMoL – https://pymol.org/ HISAT2 (2.0.5) HISAT2 https://daehwankimlab.github.io/hisat2/ 18 Cell Reports 44, 116678, December 23, 2025 Procell Life Science & Technology and were grown in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% FBS. ..

    Electroporation:

    Article Title: Amyotrophic Lateral Sclerosis-associated 3′ UTR enhancer embedded within CAV1 risk gene
    Article Snippet: .. Electroporation of SH-SY5Y cells with pGL3-Promoter (and derivatives, Promega #E1761), pGL3-Basic (Addgene #212936), pGL3-Control (Addgene #212937), and 759_Renilla (derived from pGL4.70[hRluc], Promega #E6881) was performed using the Neon ® Transfection System (Thermo Fisher) according to the manufacturer’s instructions. .. For luciferase reporter assays, transfections were performed in DMEM without phenol red (Cytiva, SH30284.01) supplemented with 10% FBS.

    Derivative Assay:

    Article Title: Amyotrophic Lateral Sclerosis-associated 3′ UTR enhancer embedded within CAV1 risk gene
    Article Snippet: .. Electroporation of SH-SY5Y cells with pGL3-Promoter (and derivatives, Promega #E1761), pGL3-Basic (Addgene #212936), pGL3-Control (Addgene #212937), and 759_Renilla (derived from pGL4.70[hRluc], Promega #E6881) was performed using the Neon ® Transfection System (Thermo Fisher) according to the manufacturer’s instructions. .. For luciferase reporter assays, transfections were performed in DMEM without phenol red (Cytiva, SH30284.01) supplemented with 10% FBS.

    Transfection:

    Article Title: Amyotrophic Lateral Sclerosis-associated 3′ UTR enhancer embedded within CAV1 risk gene
    Article Snippet: .. Electroporation of SH-SY5Y cells with pGL3-Promoter (and derivatives, Promega #E1761), pGL3-Basic (Addgene #212936), pGL3-Control (Addgene #212937), and 759_Renilla (derived from pGL4.70[hRluc], Promega #E6881) was performed using the Neon ® Transfection System (Thermo Fisher) according to the manufacturer’s instructions. .. For luciferase reporter assays, transfections were performed in DMEM without phenol red (Cytiva, SH30284.01) supplemented with 10% FBS.

    Expressing:

    Article Title: Bone Metastatic Progression of Prostate Cancer is Regulated by TRIM28-LDHA Mediated Metabolism
    Article Snippet: LDHA promoter luciferase reporter assays were conducted according to the manual of Dual-Luciferase Reporter Assay System from Promega. .. Briefly, C4–2B cells were seeded in a 24-well plate and co-transfected with the Renilla expression plasmid pRL-TK (RRID:Addgene_27163) and the reporter constructs for LDHA promoter in pGL3 vector (RRID:Addgene_212937). ..

    Construct:

    Article Title: Bone Metastatic Progression of Prostate Cancer is Regulated by TRIM28-LDHA Mediated Metabolism
    Article Snippet: LDHA promoter luciferase reporter assays were conducted according to the manual of Dual-Luciferase Reporter Assay System from Promega. .. Briefly, C4–2B cells were seeded in a 24-well plate and co-transfected with the Renilla expression plasmid pRL-TK (RRID:Addgene_27163) and the reporter constructs for LDHA promoter in pGL3 vector (RRID:Addgene_212937). ..

    Clone Assay:

    Article Title: UHRF1 restricts HCoV-229E infection through epigenetic silencing of the viral receptor APN
    Article Snippet: A Chemiluminescent EMSA kit (Beyotime #GS009) was used to detect interactions between the probes and nuclear proteins extracted from control and UHRF1 -knockout A549 cells using NE-PERTM Nuclear and Cytoplasmic Extraction Reagents (Thermo #78833). .. The APN promoter sequences (−153 to −1) were cloned into the pGL3 Basic vector (Addgene ##212936), resulting in the plasmid pGL3-APN-Luc. .. The pGL3-APN-Luc plasmid was methylated in vitro using CpG Methyltransferase M.SssI (NEB #M0226S).

    Luciferase:

    Article Title: tRF-21 LeuTAA Promotes Oxidative Stress by Altering Glutathione Metabolic Enzymes to Support Prostate Cancer Progression
    Article Snippet: Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, and Reactome analyses and visualization were performed using OmicShare ( https://www.omicshare.com ) and SangerBox ( http://www.sangerbox.com/ ). .. The firefly luciferase–expressing plasmids pGL3-basic (RRID:Addgene_212936), pGL3-promoter (RRID:Addgene_172006), and Renilla pRL-CMV (RRID:Addgene_41046) were purchased from Promega (TM033, E2261). ..

    Article Title: Activation of WDHD1 by DNA demethylases promotes MINPP1 transcription and glycolysis in lung adenocarcinoma progression
    Article Snippet: .. The MINPP1 promoter (chr10: 87504645–87504992) obtained from UCSC ( https://genome.ucsc.edu/index.html ) was amplified and inserted into the pGL3 BasicVector (212936, Addgene, Watertown, MA, USA) between the SacI and HindIII sites. pRL Renilla Luciferase Control Reporter Vectors (E2231, Promega Corporation, Madison, WI, USA) were used as a control. ..

    Amplification:

    Article Title: Activation of WDHD1 by DNA demethylases promotes MINPP1 transcription and glycolysis in lung adenocarcinoma progression
    Article Snippet: .. The MINPP1 promoter (chr10: 87504645–87504992) obtained from UCSC ( https://genome.ucsc.edu/index.html ) was amplified and inserted into the pGL3 BasicVector (212936, Addgene, Watertown, MA, USA) between the SacI and HindIII sites. pRL Renilla Luciferase Control Reporter Vectors (E2231, Promega Corporation, Madison, WI, USA) were used as a control. ..

    Control:

    Article Title: Activation of WDHD1 by DNA demethylases promotes MINPP1 transcription and glycolysis in lung adenocarcinoma progression
    Article Snippet: .. The MINPP1 promoter (chr10: 87504645–87504992) obtained from UCSC ( https://genome.ucsc.edu/index.html ) was amplified and inserted into the pGL3 BasicVector (212936, Addgene, Watertown, MA, USA) between the SacI and HindIII sites. pRL Renilla Luciferase Control Reporter Vectors (E2231, Promega Corporation, Madison, WI, USA) were used as a control. ..



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    Addgene inc pgl3 basic luciferase reporter
    Estrogen promotes HNRNPAB expression via SP1. (A) Immunoblot assessment of HNRNPAB in 2 human normal breast epithelial cell lines and 11 human BC cell lines. (B) CPTAC database analyzed the relative HNRNPAB and ERα protein level in 105 BC patients. P value was determined by Pearson correlation analysis. (C) The relative expression of TFF1 and HNRNPAB mRNAs after stimulated with 10 nM E 2 in estrogen-deprived MCF-7 cells for 48 h analyzed by qRT-PCR. (D) Immunoblot assessment of HNRNPAB expression in MCF-7 with or without 10 nM E 2 in estrogen-deprived MCF-7 cells for 72 h, or in short-term oestrogen deprivation (STED) MCF-7 cells for 7 days and parental cells. (E) The schematic of HNRNPAB promoter region sequence selected from the transcription start site of -2 kb~+100 bp. (F) MCF-7 cells were transfected with <t>pGL3</t> basic reporter vector containing HNRNPAB promoter, and pRL-TK reporter control vector containing luciferase activity, as well as control siRNA or different siRNA sequences of JUN , FOS , FOXA1 and SP1 . The relative fluorescence activity was measured. (G) CPTAC database analyzed the relative HNRNPAB and SP1 protein level in 68 ER+ BC patients. P value was determined by Pearson correlation analysis. (H) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector containing different regions of HNRNPAB promoter. The relative fluorescence activity was measured. (I) The schematic of three predicted conserved SP1 binding sites on the upstream -425 bp~+100 bp regions of the human HNRNPAB gene. Red boxes represent the predicted SP1 binding sites. (J) The DNA regions enriched by SP1 in ChIP assay were verified by PCR. (K) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector or containing “b” or “b” mutant regions. The relative fluorescence activity was measured. (L) The relative expression of SP1 and HNRNPAB mRNAs in MCF-7 cells bearing control or SP1 shRNAs analyzed by qRT-PCR. (M) Immunoblot assessment of SP1 and HNRNPAB expression in MCF-7 cells with or without SP1 shRNAs in the presence or absence of 10 nM E 2 for 48 h. Data was shown as mean ± S.D. from three independent experiments. Unpaired two-tailed Student's t test (C, H, K) and one-way ANOVA followed by Tukey's multiple comparisons test (F, L). ns, P >0.05; ***, P <0.001; ****, P <0.0001.
    Pgl3 Basic Luciferase Reporter, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Estrogen promotes HNRNPAB expression via SP1. (A) Immunoblot assessment of HNRNPAB in 2 human normal breast epithelial cell lines and 11 human BC cell lines. (B) CPTAC database analyzed the relative HNRNPAB and ERα protein level in 105 BC patients. P value was determined by Pearson correlation analysis. (C) The relative expression of TFF1 and HNRNPAB mRNAs after stimulated with 10 nM E 2 in estrogen-deprived MCF-7 cells for 48 h analyzed by qRT-PCR. (D) Immunoblot assessment of HNRNPAB expression in MCF-7 with or without 10 nM E 2 in estrogen-deprived MCF-7 cells for 72 h, or in short-term oestrogen deprivation (STED) MCF-7 cells for 7 days and parental cells. (E) The schematic of HNRNPAB promoter region sequence selected from the transcription start site of -2 kb~+100 bp. (F) MCF-7 cells were transfected with pGL3 basic reporter vector containing HNRNPAB promoter, and pRL-TK reporter control vector containing luciferase activity, as well as control siRNA or different siRNA sequences of JUN , FOS , FOXA1 and SP1 . The relative fluorescence activity was measured. (G) CPTAC database analyzed the relative HNRNPAB and SP1 protein level in 68 ER+ BC patients. P value was determined by Pearson correlation analysis. (H) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector containing different regions of HNRNPAB promoter. The relative fluorescence activity was measured. (I) The schematic of three predicted conserved SP1 binding sites on the upstream -425 bp~+100 bp regions of the human HNRNPAB gene. Red boxes represent the predicted SP1 binding sites. (J) The DNA regions enriched by SP1 in ChIP assay were verified by PCR. (K) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector or containing “b” or “b” mutant regions. The relative fluorescence activity was measured. (L) The relative expression of SP1 and HNRNPAB mRNAs in MCF-7 cells bearing control or SP1 shRNAs analyzed by qRT-PCR. (M) Immunoblot assessment of SP1 and HNRNPAB expression in MCF-7 cells with or without SP1 shRNAs in the presence or absence of 10 nM E 2 for 48 h. Data was shown as mean ± S.D. from three independent experiments. Unpaired two-tailed Student's t test (C, H, K) and one-way ANOVA followed by Tukey's multiple comparisons test (F, L). ns, P >0.05; ***, P <0.001; ****, P <0.0001.

    Journal: International Journal of Biological Sciences

    Article Title: The Interaction of CircESR1 and HNRNPAB Regulates Cell Cycle Transition of Breast Cancer Cell

    doi: 10.7150/ijbs.126014

    Figure Lengend Snippet: Estrogen promotes HNRNPAB expression via SP1. (A) Immunoblot assessment of HNRNPAB in 2 human normal breast epithelial cell lines and 11 human BC cell lines. (B) CPTAC database analyzed the relative HNRNPAB and ERα protein level in 105 BC patients. P value was determined by Pearson correlation analysis. (C) The relative expression of TFF1 and HNRNPAB mRNAs after stimulated with 10 nM E 2 in estrogen-deprived MCF-7 cells for 48 h analyzed by qRT-PCR. (D) Immunoblot assessment of HNRNPAB expression in MCF-7 with or without 10 nM E 2 in estrogen-deprived MCF-7 cells for 72 h, or in short-term oestrogen deprivation (STED) MCF-7 cells for 7 days and parental cells. (E) The schematic of HNRNPAB promoter region sequence selected from the transcription start site of -2 kb~+100 bp. (F) MCF-7 cells were transfected with pGL3 basic reporter vector containing HNRNPAB promoter, and pRL-TK reporter control vector containing luciferase activity, as well as control siRNA or different siRNA sequences of JUN , FOS , FOXA1 and SP1 . The relative fluorescence activity was measured. (G) CPTAC database analyzed the relative HNRNPAB and SP1 protein level in 68 ER+ BC patients. P value was determined by Pearson correlation analysis. (H) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector containing different regions of HNRNPAB promoter. The relative fluorescence activity was measured. (I) The schematic of three predicted conserved SP1 binding sites on the upstream -425 bp~+100 bp regions of the human HNRNPAB gene. Red boxes represent the predicted SP1 binding sites. (J) The DNA regions enriched by SP1 in ChIP assay were verified by PCR. (K) 293T cells were transfected with control or SP1 vector, and pRL-TK reporter control vector containing luciferase activity, as well as pGL3 basic reporter vector or containing “b” or “b” mutant regions. The relative fluorescence activity was measured. (L) The relative expression of SP1 and HNRNPAB mRNAs in MCF-7 cells bearing control or SP1 shRNAs analyzed by qRT-PCR. (M) Immunoblot assessment of SP1 and HNRNPAB expression in MCF-7 cells with or without SP1 shRNAs in the presence or absence of 10 nM E 2 for 48 h. Data was shown as mean ± S.D. from three independent experiments. Unpaired two-tailed Student's t test (C, H, K) and one-way ANOVA followed by Tukey's multiple comparisons test (F, L). ns, P >0.05; ***, P <0.001; ****, P <0.0001.

    Article Snippet: For transcription factor mediated HNRNPAB expression, 0.2 μg pGL3 Basic luciferase reporter (RRID: Addgene_48743), 50 nmol JUN or FOS or FOXA1 or SP1 siRNAs and 0.02 μg pRL-TK plasmid (RRID: Addgene_11313) were transfected into cells using Lipofectamine 2000 (Invitrogen, Carlsbad, USA).

    Techniques: Expressing, Western Blot, Quantitative RT-PCR, Sequencing, Transfection, Plasmid Preparation, Control, Luciferase, Activity Assay, Fluorescence, Binding Assay, Mutagenesis, Two Tailed Test