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Promega pgl3 luciferase vectors
Pgl3 Luciferase Vectors, 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/product/pgl3+luciferase+vectors/pgl3+basic/pm40664766-81-25-28
Average 90 stars, based on 1 article reviews
pgl3 luciferase vectors - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Binding Assay:

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR‐1236/HER2 signaling pathway
Article Snippet: .. The fragments containing the predicted binding sites for miR‐1236 in circ0030018 sequence and HER2 3’‐UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild‐type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR‐1236 were constructed by Fast Site‐Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: CircRNA ZFR promotes cell progression by regulating miR-96a-5p/SLC1A1 axis in hepatocellular carcinoma.
Article Snippet: The blots were then incubated with HRP secondary antibodies (Dilution: 1: 6000, Aspen, China) for 2 h at room temperature and the bands visualized using enhanced chemiluminescence detection system and a Chemidoc XRS imager system (Bio-Rad Laboratories, USA). .. The wild-type (WT) or mutated (MUT) circRNA ZFR or 30-untranslated region (30-UTR) region of SLC1A1 containing miR-96a-5p specific binding sites were amplified and sub-cloned into pGL3 luciferase vectors (Promega, Madison, WI), namely pGL3-circRNAZFR-WT (circRNA ZFR -WT), pGL3-circRNA ZFR-MUT (circRNAZFR-MUT), pGL3-SLC1A1-WT (SLC1A1-WT), and pGL3- SLC1A1-MUT (SLC1A1-MUT). .. For luciferase reporter assay, 293 T cells were seeded into 96-well plates (2 × 103 cells/well) and cotransfected with luciferase reporter plasmids and miR-96a-5p or miR-con using Lipofectamine 2000 reagent (Invitrogen).

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR-1236/HER2 signaling pathway.
Article Snippet: .. The fragments containing the predicted binding sites for miR-1236 in circ0030018 sequence and HER2 3’-UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild-type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR1236 were constructed by Fast Site-Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Sequencing:

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR‐1236/HER2 signaling pathway
Article Snippet: .. The fragments containing the predicted binding sites for miR‐1236 in circ0030018 sequence and HER2 3’‐UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild‐type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR‐1236 were constructed by Fast Site‐Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR-1236/HER2 signaling pathway.
Article Snippet: .. The fragments containing the predicted binding sites for miR-1236 in circ0030018 sequence and HER2 3’-UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild-type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR1236 were constructed by Fast Site-Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Synthesized:

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR‐1236/HER2 signaling pathway
Article Snippet: .. The fragments containing the predicted binding sites for miR‐1236 in circ0030018 sequence and HER2 3’‐UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild‐type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR‐1236 were constructed by Fast Site‐Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR-1236/HER2 signaling pathway.
Article Snippet: .. The fragments containing the predicted binding sites for miR-1236 in circ0030018 sequence and HER2 3’-UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild-type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR1236 were constructed by Fast Site-Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Caspase-3 activity assay Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. Luciferase reporter assay The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Luciferase:

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR‐1236/HER2 signaling pathway
Article Snippet: .. The fragments containing the predicted binding sites for miR‐1236 in circ0030018 sequence and HER2 3’‐UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild‐type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR‐1236 were constructed by Fast Site‐Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Article Title: CircRNA ZFR promotes cell progression by regulating miR-96a-5p/SLC1A1 axis in hepatocellular carcinoma.
Article Snippet: The blots were then incubated with HRP secondary antibodies (Dilution: 1: 6000, Aspen, China) for 2 h at room temperature and the bands visualized using enhanced chemiluminescence detection system and a Chemidoc XRS imager system (Bio-Rad Laboratories, USA). .. The wild-type (WT) or mutated (MUT) circRNA ZFR or 30-untranslated region (30-UTR) region of SLC1A1 containing miR-96a-5p specific binding sites were amplified and sub-cloned into pGL3 luciferase vectors (Promega, Madison, WI), namely pGL3-circRNAZFR-WT (circRNA ZFR -WT), pGL3-circRNA ZFR-MUT (circRNAZFR-MUT), pGL3-SLC1A1-WT (SLC1A1-WT), and pGL3- SLC1A1-MUT (SLC1A1-MUT). .. For luciferase reporter assay, 293 T cells were seeded into 96-well plates (2 × 103 cells/well) and cotransfected with luciferase reporter plasmids and miR-96a-5p or miR-con using Lipofectamine 2000 reagent (Invitrogen).

Article Title: Overexpression of LINC00607 inhibits cell growth and aggressiveness by regulating the miR-1289/EFNA5 axis in non-small-cell lung cancer
Article Snippet: Cell lysates and biotinylated RNAs were incubated with streptavidin-coated magnetic beads (Life Technologies) at 4°C for 3 h. Finally, RNA–protein binding mixture was purified and then detected by RT-qPCR. .. The wild-type (WT) LINC00607 and 3′-untranslated regions of WT EFNA5 were subcloned into pGL3 luciferase vectors (Promega) and named as LINC00607-WT and EFNA5-WT. .. Their mutant-type (MUT) controls were also constructed by using a Phusion Site-Directed Mutagenesis Kit (Thermo Fisher Scientific) and named as LINC00607-MUT and EFNA5-MUT.

Article Title: miR-146a-5p regulates autophagy and NLRP3 inflammasome activation in epithelial barrier damage in the in vitro cell model of ulcerative colitis through the RNF8/Notch1/mTORC1 pathway.
Article Snippet: Ulcerative colitis (UC) is a chronic inflammatory disease affecting the colon that can be influenced by microRNAs (miRNAs).. This study aims to investigate the impact of miR-146a-5p on lipopolysaccharide (LPS)-induced Caco2/HT-29 cell autophagy and NLRP3 inflammasome activation and the underlying mechanism, with the aim of identifying potential therapeutic targets.. We used LPS to establish Caco-2/HT-29 cell models and measured cell viability by CCK-8.

Article Title: Human umbilical cord mesenchymal stem cell-derived extracellular vesicles improve ovarian function in rats with primary ovarian insufficiency by carrying miR-145-5p.
Article Snippet: Objective: Stem cell/exosome therapy is a novel strategy for primary ovarian insufficiency (POI).. This paper is to examine the role of human umbilical cord mesenchymal stem cell-derived extracellular vesicles (hUCMSC-EVs)

Article Title: Isoliquiritigenin inhibits circ0030018 to suppress glioma tumorigenesis via the miR-1236/HER2 signaling pathway.
Article Snippet: .. The fragments containing the predicted binding sites for miR-1236 in circ0030018 sequence and HER2 3’-UTR were synthesized and inserted to the pGL3 luciferase vectors (Promega, USA) downstream of the luciferase immediately, served as wild-type vectors (wt). .. The mutant vectors with mutations in the predicted binding sites for miR1236 were constructed by Fast Site-Directed Mutagenesis Kit (TIANGEN, China) and served as mutant controls (mut).

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Caspase-3 activity assay Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. Luciferase reporter assay The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Mutagenesis:

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Article Title: miR-146a-5p regulates autophagy and NLRP3 inflammasome activation in epithelial barrier damage in the in vitro cell model of ulcerative colitis through the RNF8/Notch1/mTORC1 pathway.
Article Snippet: Ulcerative colitis (UC) is a chronic inflammatory disease affecting the colon that can be influenced by microRNAs (miRNAs).. This study aims to investigate the impact of miR-146a-5p on lipopolysaccharide (LPS)-induced Caco2/HT-29 cell autophagy and NLRP3 inflammasome activation and the underlying mechanism, with the aim of identifying potential therapeutic targets.. We used LPS to establish Caco-2/HT-29 cell models and measured cell viability by CCK-8.

Article Title: Human umbilical cord mesenchymal stem cell-derived extracellular vesicles improve ovarian function in rats with primary ovarian insufficiency by carrying miR-145-5p.
Article Snippet: Objective: Stem cell/exosome therapy is a novel strategy for primary ovarian insufficiency (POI).. This paper is to examine the role of human umbilical cord mesenchymal stem cell-derived extracellular vesicles (hUCMSC-EVs)

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Caspase-3 activity assay Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. Luciferase reporter assay The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Clone Assay:

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Article Title: miR-146a-5p regulates autophagy and NLRP3 inflammasome activation in epithelial barrier damage in the in vitro cell model of ulcerative colitis through the RNF8/Notch1/mTORC1 pathway.
Article Snippet: Ulcerative colitis (UC) is a chronic inflammatory disease affecting the colon that can be influenced by microRNAs (miRNAs).. This study aims to investigate the impact of miR-146a-5p on lipopolysaccharide (LPS)-induced Caco2/HT-29 cell autophagy and NLRP3 inflammasome activation and the underlying mechanism, with the aim of identifying potential therapeutic targets.. We used LPS to establish Caco-2/HT-29 cell models and measured cell viability by CCK-8.

Article Title: Human umbilical cord mesenchymal stem cell-derived extracellular vesicles improve ovarian function in rats with primary ovarian insufficiency by carrying miR-145-5p.
Article Snippet: Objective: Stem cell/exosome therapy is a novel strategy for primary ovarian insufficiency (POI).. This paper is to examine the role of human umbilical cord mesenchymal stem cell-derived extracellular vesicles (hUCMSC-EVs)

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Caspase-3 activity assay Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. Luciferase reporter assay The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..

Amplification:

Article Title: CircRNA ZFR promotes cell progression by regulating miR-96a-5p/SLC1A1 axis in hepatocellular carcinoma.
Article Snippet: The blots were then incubated with HRP secondary antibodies (Dilution: 1: 6000, Aspen, China) for 2 h at room temperature and the bands visualized using enhanced chemiluminescence detection system and a Chemidoc XRS imager system (Bio-Rad Laboratories, USA). .. The wild-type (WT) or mutated (MUT) circRNA ZFR or 30-untranslated region (30-UTR) region of SLC1A1 containing miR-96a-5p specific binding sites were amplified and sub-cloned into pGL3 luciferase vectors (Promega, Madison, WI), namely pGL3-circRNAZFR-WT (circRNA ZFR -WT), pGL3-circRNA ZFR-MUT (circRNAZFR-MUT), pGL3-SLC1A1-WT (SLC1A1-WT), and pGL3- SLC1A1-MUT (SLC1A1-MUT). .. For luciferase reporter assay, 293 T cells were seeded into 96-well plates (2 × 103 cells/well) and cotransfected with luciferase reporter plasmids and miR-96a-5p or miR-con using Lipofectamine 2000 reagent (Invitrogen).

Reporter Assay:

Article Title: miR-29c-3p Attenuates β-Amyloid-Induced Neurotoxicity in Alzheimer’s Disease Through Regulating β-Site Amyloid Precursor Protein-Cleaving Enzyme 1
Article Snippet: Caspase-3 activity assay Transfected PC12 cells were treated with 10 μM Aβ for 24 h. The absorbance was measured at 405nm using a microplate reader (Becton Dickinson, Mountain View, CA, USA) using the caspase-3 assay Kit (Solarbio, Beijing, China). .. Luciferase reporter assay The wild type or mutant-type 3′-UTR of BACE1 sequences containing putative miR-29c-3p-binding sites were synthesized and cloned into pGL3 luciferase vectors (Promega, Madison, Wisconsin, USA), creating pGL3-BACE1-Wt (Wt) or pGL3- BACE1-Mut (Mut) reporter vectors. ..



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