Review




Structured Review

Sangon Biotech pgl3 basic luciferase reporter plasmid
Pgl3 Basic Luciferase Reporter Plasmid, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/assay+bca+kit+protein/pmc12910405-316-13-18
Average 86 stars, based on 1 article reviews
pgl3 basic luciferase reporter plasmid - by Bioz Stars, 2026-10
86/100 stars

Images

Related Articles

Plasmid Preparation:

Article Title: ACSL5 promotes lipid deposition and lipoapoptosis in proximal tubular epithelial cells of diabetic kidney disease.
Article Snippet: Background: Lipoapoptosis in Proximal tubular epithelial cells (PTCs) are substantial in the etiology of diabetic kidney disease (DKD), yet the underlying mechanisms warrant further investigation.. Acyl-CoA synthetase longchain family member 5 (ACSL5) facilitates the formation of acyl-CoA, however, the precise role of ACSL5 in lipoapoptosis of PTCs in DKD remains inconclusive.. Methods: Transcriptomic data analysis identified the hub gene Acsl5 associated with lipid metabolism in DKD.

Article Title: Blockade of endothelial adenosine receptor 2A suppresses atherosclerosis in vivo through inhibiting CREB-ALK5-mediated endothelial to mesenchymal transition
Article Snippet: Cells were seed in 96-well plates and transfected with 100 ng constructed reporter plasmids using Lipofectamine 2000 (#11668019, Thermo Fisher Scientific, USA) according to the manufacturer’s instructions. .. To construct the ALK5 promoter reporter plasmid, a 2143 bp fragment of the ALK5 gene promoter (−1960/+183 relative to the transcription start site) was amplified using PCR and then inserted into the pGL3-basic plasmid (Sangon Biotech, Shanghai, China) at specific sites ( KpnI and XhoI ), resulting in the generation of pGL3–1960. ..

Article Title: SIX2 ‐Mediated Microglial M2 Polarization and Exosomal miR ‐3470b Delivery Protect Dopaminergic Neurons in Parkinson's Disease
Article Snippet: The Dual‐LumiTM Luciferase Reporter Gene Assay kit was obtained from Beyotime Biotechnology (Shanghai, China). .. The promoter region of the mouse DDIT4 and GREM1 gene was subcloned into pGL3 Basic luciferase reporter plasmid (Sangon Biotech, Shanghai, China). ..

Luciferase:

Article Title: ACSL5 promotes lipid deposition and lipoapoptosis in proximal tubular epithelial cells of diabetic kidney disease.
Article Snippet: Background: Lipoapoptosis in Proximal tubular epithelial cells (PTCs) are substantial in the etiology of diabetic kidney disease (DKD), yet the underlying mechanisms warrant further investigation.. Acyl-CoA synthetase longchain family member 5 (ACSL5) facilitates the formation of acyl-CoA, however, the precise role of ACSL5 in lipoapoptosis of PTCs in DKD remains inconclusive.. Methods: Transcriptomic data analysis identified the hub gene Acsl5 associated with lipid metabolism in DKD.

Article Title: miR-93-5p/IFNAR1 axis promotes gastric cancer metastasis through activating the STAT3 signaling pathway.
Article Snippet: Aberrant expression of microRNAs (miRNAs) plays an important role in gastric cancer (GC) development. miR-93-5p has shown opposing functions in different types of cancers, but the exact expression pattern and molecular mechanism of miR-93-5p in GC development remain to be elucidated.. Here, we reported that miR-93-5p expression was increased in GC tissues compared with the adjacent normal tissues and that its overexpression was correlated with distant metastasis and poor survival in GC patients. miR-935p knockdown inhibited the migration, invasion and proliferation of GC cells in vitro and in vivo, while its overexpression displayed an opposite result.. Using an mRNA microarray, we found that miR-93-5p significantly downregulated IFNAR1 expression in GC cells, which was further identified as a direct target of miR-93-5p.

Article Title: Melatonin attenuates low shear stress-induced pyroptosis and endothelial cell dysfunction via the RORα/miR-223/STAT-3 signalling pathway
Article Snippet: .. Luciferase reporter plasmids (pGL3-basic; Sangon Biotech Co., Ltd.) were constructed with full-length or truncated promoters of miR-223. .. In addition, the full-length RORα gene was cloned into the pcDNA3.0 (Sangon Biotech Co., Ltd.) plasmid to overexpress RORα.

Article Title: SIX2 ‐Mediated Microglial M2 Polarization and Exosomal miR ‐3470b Delivery Protect Dopaminergic Neurons in Parkinson's Disease
Article Snippet: The Dual‐LumiTM Luciferase Reporter Gene Assay kit was obtained from Beyotime Biotechnology (Shanghai, China). .. The promoter region of the mouse DDIT4 and GREM1 gene was subcloned into pGL3 Basic luciferase reporter plasmid (Sangon Biotech, Shanghai, China). ..

Reporter Assay:

Article Title: miR-93-5p/IFNAR1 axis promotes gastric cancer metastasis through activating the STAT3 signaling pathway.
Article Snippet: Aberrant expression of microRNAs (miRNAs) plays an important role in gastric cancer (GC) development. miR-93-5p has shown opposing functions in different types of cancers, but the exact expression pattern and molecular mechanism of miR-93-5p in GC development remain to be elucidated.. Here, we reported that miR-93-5p expression was increased in GC tissues compared with the adjacent normal tissues and that its overexpression was correlated with distant metastasis and poor survival in GC patients. miR-935p knockdown inhibited the migration, invasion and proliferation of GC cells in vitro and in vivo, while its overexpression displayed an opposite result.. Using an mRNA microarray, we found that miR-93-5p significantly downregulated IFNAR1 expression in GC cells, which was further identified as a direct target of miR-93-5p.

Mutagenesis:

Article Title: miR-93-5p/IFNAR1 axis promotes gastric cancer metastasis through activating the STAT3 signaling pathway.
Article Snippet: Aberrant expression of microRNAs (miRNAs) plays an important role in gastric cancer (GC) development. miR-93-5p has shown opposing functions in different types of cancers, but the exact expression pattern and molecular mechanism of miR-93-5p in GC development remain to be elucidated.. Here, we reported that miR-93-5p expression was increased in GC tissues compared with the adjacent normal tissues and that its overexpression was correlated with distant metastasis and poor survival in GC patients. miR-935p knockdown inhibited the migration, invasion and proliferation of GC cells in vitro and in vivo, while its overexpression displayed an opposite result.. Using an mRNA microarray, we found that miR-93-5p significantly downregulated IFNAR1 expression in GC cells, which was further identified as a direct target of miR-93-5p.

Synthesized:

Article Title: miR-93-5p/IFNAR1 axis promotes gastric cancer metastasis through activating the STAT3 signaling pathway.
Article Snippet: Aberrant expression of microRNAs (miRNAs) plays an important role in gastric cancer (GC) development. miR-93-5p has shown opposing functions in different types of cancers, but the exact expression pattern and molecular mechanism of miR-93-5p in GC development remain to be elucidated.. Here, we reported that miR-93-5p expression was increased in GC tissues compared with the adjacent normal tissues and that its overexpression was correlated with distant metastasis and poor survival in GC patients. miR-935p knockdown inhibited the migration, invasion and proliferation of GC cells in vitro and in vivo, while its overexpression displayed an opposite result.. Using an mRNA microarray, we found that miR-93-5p significantly downregulated IFNAR1 expression in GC cells, which was further identified as a direct target of miR-93-5p.

Construct:

Article Title: Melatonin attenuates low shear stress-induced pyroptosis and endothelial cell dysfunction via the RORα/miR-223/STAT-3 signalling pathway
Article Snippet: .. Luciferase reporter plasmids (pGL3-basic; Sangon Biotech Co., Ltd.) were constructed with full-length or truncated promoters of miR-223. .. In addition, the full-length RORα gene was cloned into the pcDNA3.0 (Sangon Biotech Co., Ltd.) plasmid to overexpress RORα.

Article Title: Blockade of endothelial adenosine receptor 2A suppresses atherosclerosis in vivo through inhibiting CREB-ALK5-mediated endothelial to mesenchymal transition
Article Snippet: Cells were seed in 96-well plates and transfected with 100 ng constructed reporter plasmids using Lipofectamine 2000 (#11668019, Thermo Fisher Scientific, USA) according to the manufacturer’s instructions. .. To construct the ALK5 promoter reporter plasmid, a 2143 bp fragment of the ALK5 gene promoter (−1960/+183 relative to the transcription start site) was amplified using PCR and then inserted into the pGL3-basic plasmid (Sangon Biotech, Shanghai, China) at specific sites ( KpnI and XhoI ), resulting in the generation of pGL3–1960. ..

Amplification:

Article Title: Blockade of endothelial adenosine receptor 2A suppresses atherosclerosis in vivo through inhibiting CREB-ALK5-mediated endothelial to mesenchymal transition
Article Snippet: Cells were seed in 96-well plates and transfected with 100 ng constructed reporter plasmids using Lipofectamine 2000 (#11668019, Thermo Fisher Scientific, USA) according to the manufacturer’s instructions. .. To construct the ALK5 promoter reporter plasmid, a 2143 bp fragment of the ALK5 gene promoter (−1960/+183 relative to the transcription start site) was amplified using PCR and then inserted into the pGL3-basic plasmid (Sangon Biotech, Shanghai, China) at specific sites ( KpnI and XhoI ), resulting in the generation of pGL3–1960. ..

Polymerase Chain Reaction:

Article Title: Blockade of endothelial adenosine receptor 2A suppresses atherosclerosis in vivo through inhibiting CREB-ALK5-mediated endothelial to mesenchymal transition
Article Snippet: Cells were seed in 96-well plates and transfected with 100 ng constructed reporter plasmids using Lipofectamine 2000 (#11668019, Thermo Fisher Scientific, USA) according to the manufacturer’s instructions. .. To construct the ALK5 promoter reporter plasmid, a 2143 bp fragment of the ALK5 gene promoter (−1960/+183 relative to the transcription start site) was amplified using PCR and then inserted into the pGL3-basic plasmid (Sangon Biotech, Shanghai, China) at specific sites ( KpnI and XhoI ), resulting in the generation of pGL3–1960. ..



Similar Products

95
Addgene inc pgl3 basic 180 luciferase reporter plasmid
Pgl3 Basic 180 Luciferase Reporter Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/pGL3+(-BRE)+Luciferase+(Plasmid+%2345127)/10__1158_slash_0008___5472__can___25___2893-63-26-31
Average 95 stars, based on 1 article reviews
pgl3 basic 180 luciferase reporter plasmid - by Bioz Stars, 2026-10
95/100 stars
  Buy from Supplier

86
Sangon Biotech pgl3 basic luciferase reporter plasmid
Pgl3 Basic Luciferase Reporter Plasmid, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/assay+bca+kit+protein/pmc12910405-316-13-18
Average 86 stars, based on 1 article reviews
pgl3 basic luciferase reporter plasmid - by Bioz Stars, 2026-10
86/100 stars
  Buy from Supplier

93
Addgene inc pgl3 basic
Pgl3 Basic, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/pGL3+Basic+Control+Vector+(Plasmid+%23137707)/pm41713257-68-22-27
Average 93 stars, based on 1 article reviews
pgl3 basic - by Bioz Stars, 2026-10
93/100 stars
  Buy from Supplier

93
Addgene inc pgl3 basic vector
Pgl3 Basic Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/pGL3+Basic+Control+Vector+(Plasmid+%23137707)/pmc12893712-79-26-28
Average 93 stars, based on 1 article reviews
pgl3 basic vector - by Bioz Stars, 2026-10
93/100 stars
  Buy from Supplier

95
Addgene inc pgl3 basic luciferase reporter plasmid
Pgl3 Basic Luciferase Reporter Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pgl3-basic+plasmid/pGL3+(-BRE)+Luciferase+(Plasmid+%2345127)/pmc12757066-200-18-22
Average 95 stars, based on 1 article reviews
pgl3 basic luciferase reporter plasmid - by Bioz Stars, 2026-10
95/100 stars
  Buy from Supplier

94
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
https://www.bioz.com/product/pgl3-basic+plasmid/pGL3+(Plasmid+%2348743)/pmc12839121-155-8-13
Average 94 stars, based on 1 article reviews
pgl3 basic luciferase reporter - by Bioz Stars, 2026-10
94/100 stars
  Buy from Supplier

Image Search Results


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