Review



pgl3-basic firefly luciferase expression vector  (Promega)

 
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Promega pgl3-basic firefly luciferase expression vector
    Pgl3 Basic Firefly Luciferase Expression Vector, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pm36293554-293-16-21
    Average 90 stars, based on 1 article reviews
    pgl3-basic firefly luciferase expression vector - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: An epigenetic mechanism regulates germ cell-specific expression of the porcine Deleted in Azoospermia-Like (DAZL) gene.
    Article Snippet: The Deleted in Azoospermia-Like (DAZL) gene is specifically expressed in fetal and adult gonads.. While DAZL is known to play a role during gametogenesis, the mechanisms governing its germ cell-specific expression remain unclear.. We identified the 50 untranslated region (UTR) of the porcine DAZL gene and cloned and characterized 2 kilobase pairs of its TATA-less 50 flanking region, identifying CpG-rich regions within the proximal promoter.

    Article Title: The role of prostaglandin E receptor-dependent signaling via cAMP in Mdr1b gene activation in primary rat hepatocyte cultures.
    Article Snippet: Multidrug resistance (mdr) proteins of the mdr1 type function as multispecific xenobiotic transporters in hepatocytes.. In the liver, mdr1 overexpression occurs during regeneration, cirrhosis, and hepatocarcinogenesis and may contribute to primary chemotherapy resistance.. Cultured rat hepatocytes exhibit a time-dependent “intrinsic” increase in functional mdr1b expression, which depends on cyclooxygenase-catalyzed prostaglandin E2 release.

    Article Title: Sp1 and Sp3 mediate basal and serum-induced expression of human CENP-W.
    Article Snippet: Cancer-upregulated gene 2 (CUG2), which was named since it was originally identified as a putative oncogene up-regulated in various human cancers, was recently renamed CENP-W based on the new findings that it is a component of the centromeric complex playing a crucial role in the assembly of functional kinetochore complex during mitosis.. To understand the transcriptional regulation of CENP-W, we analyzed its TATA-less promoter and identified a GC-rich putative Sp1 binding site located at -46 to -36 that was critical in CENP-W expression.. Competitive electrophoretic gel mobility shift assay using mutated oligos and supershift assays with Sp1 and Sp3 antibodies demonstrated that both proteins specifically bound to this promoter region.

    Article Title: A Functional Polymorphism in PIN1 that Prevents its Suppression by AP4 Is Associated with Delayed Onset of Alzheimer's disease
    Article Snippet: The fragment was cloned into the previously generated Pin1 promoter construct (−2300 to +1) ( Ryo et al. 2002 ) with pGL3-Basic firefly luciferase expression vector (Promega, Madison, WI).

    Article Title: Identification and Expression Analysis of Dsx and Its Positive Transcriptional Regulation of IAG in Black Tiger Shrimp ( Penaeus monodon ).
    Article Snippet: The vectors were named pGL3-basicLuc1, pGL3-basic-Luc2, pGL3-basic-Luc3, and pGL3-basic-Luc4, and each fragment was cloned into the pGL3-Basic firefly luciferase expression vector (Promega, USA) for the dual-luciferase reporter assay.

    Clone Assay:

    Article Title: Stearoyl-CoA desaturase 1 expression is downregulated in liver and udder during E. coli mastitis through enhanced expression of repressive C/EBP factors and reduced expression of the inducer SREBP1A
    Article Snippet: PCR products were first cloned into pGEM-Teasy (Promega), validated by sequencing and the inserts were then excised via the artificially introduced restriction sites. .. They were subsequently cloned into the promoter-less pGL3-basic firefly luciferase expression vector (Promega). ..

    Luciferase:

    Article Title: Stearoyl-CoA desaturase 1 expression is downregulated in liver and udder during E. coli mastitis through enhanced expression of repressive C/EBP factors and reduced expression of the inducer SREBP1A
    Article Snippet: PCR products were first cloned into pGEM-Teasy (Promega), validated by sequencing and the inserts were then excised via the artificially introduced restriction sites. .. They were subsequently cloned into the promoter-less pGL3-basic firefly luciferase expression vector (Promega). ..

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Expressing:

    Article Title: Stearoyl-CoA desaturase 1 expression is downregulated in liver and udder during E. coli mastitis through enhanced expression of repressive C/EBP factors and reduced expression of the inducer SREBP1A
    Article Snippet: PCR products were first cloned into pGEM-Teasy (Promega), validated by sequencing and the inserts were then excised via the artificially introduced restriction sites. .. They were subsequently cloned into the promoter-less pGL3-basic firefly luciferase expression vector (Promega). ..

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Plasmid Preparation:

    Article Title: Stearoyl-CoA desaturase 1 expression is downregulated in liver and udder during E. coli mastitis through enhanced expression of repressive C/EBP factors and reduced expression of the inducer SREBP1A
    Article Snippet: PCR products were first cloned into pGEM-Teasy (Promega), validated by sequencing and the inserts were then excised via the artificially introduced restriction sites. .. They were subsequently cloned into the promoter-less pGL3-basic firefly luciferase expression vector (Promega). ..

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Cloning:

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Construct:

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Generated:

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Amplification:

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. Cloning The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. Cell culture, transient transfections, and reporter gene assays MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.

    Article Title: Expression of STK11 gene and its promoter activity in MCF control and cancer cells
    Article Snippet: .. The STK11 promoter reporter construct was generated by amplifying a 3995 bp fragment of the STK11 promoter using primers STK11prom-XhoI-F 5′ CGGGAAT CTCGAG TTGGAAATTCAGTG TGTAGGGCA 3′ and STK11prom-HindIII-R 5′ AAAGCGC AAGCTT CAACAAAAACCCCA AAAGGA 3′ resulting in amplification of a product containing XhoI and HindIII restriction enzyme cleavage sites to clone into pGL3-basic firefly luciferase expression vector (Promega), forming STK11–pGL3 after enzymatic digestion. .. MCF-7 human breast cancer cells (ATCC) were maintained in 1:1 mixture of DMEM/F12 medium supplemented with 10% (v/v) FBS (Invitrogen), 1% penicillin and streptomycin.



    Similar Products

    90
    Promega pgl3-basic firefly luciferase expression vector
    Pgl3 Basic Firefly Luciferase Expression Vector, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pm36293554-293-16-21
    Average 90 stars, based on 1 article reviews
    pgl3-basic firefly luciferase expression vector - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Promega firefly luciferase expression vector (pgl3-basic vector
    Firefly Luciferase Expression Vector (Pgl3 Basic Vector, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pm32911010-285-34-40
    Average 90 stars, based on 1 article reviews
    firefly luciferase expression vector (pgl3-basic vector - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Promega pgl3 basic vector expressing firefly luciferase reporter gene
    The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and <t>pGL3-basic,</t> inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05
    Pgl3 Basic Vector Expressing Firefly Luciferase Reporter Gene, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pmc07233317-94-11-14
    Average 90 stars, based on 1 article reviews
    pgl3 basic vector expressing firefly luciferase reporter gene - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Promega pgl3-basic control vector expressing firefly luciferase under sv40 promoter
    The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and <t>pGL3-basic,</t> inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05
    Pgl3 Basic Control Vector Expressing Firefly Luciferase Under Sv40 Promoter, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pmc07790267-303-16-21
    Average 90 stars, based on 1 article reviews
    pgl3-basic control vector expressing firefly luciferase under sv40 promoter - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Promega firefly luciferase expression vector (pgl3 basic
    The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and <t>pGL3-basic,</t> inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05
    Firefly Luciferase Expression Vector (Pgl3 Basic, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pmc04566942-160-13-19
    Average 90 stars, based on 1 article reviews
    firefly luciferase expression vector (pgl3 basic - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Promega pgl3-basic vector expressing firefly luciferase (luc) gene
    The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and <t>pGL3-basic,</t> inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05
    Pgl3 Basic Vector Expressing Firefly Luciferase (Luc) Gene, 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-basic+firefly+luciferase+expression+vector/pgl3+basic/pm23647419-51-14-22
    Average 90 stars, based on 1 article reviews
    pgl3-basic vector expressing firefly luciferase (luc) gene - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and pGL3-basic, inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05

    Journal: Toxicology Research

    Article Title: Suppression of LINC00460 mediated the sensitization of HCT116 cells to ionizing radiation by inhibiting epithelial–mesenchymal transition

    doi: 10.1093/toxres/tfaa010

    Figure Lengend Snippet: The essential region, which regulates LINC00460 transcription in response to irradiation, is located −145 and −44 bp upstream of LINC00460. (A) A schematic representation of the full-length LINC00460 promoter and pGL3-basic, inserted upstream of the luciferase reporter plasmid. The indicated plasmids were transfected into HCT116 cells. Luciferase assays were performed according to the manufacturer’s instructions. The percentage of luciferase activity elicited by a particular deletion construct is presented relative to the activity of the full-length LINC00460 promoter-luciferase construct. Each bar represents the mean and SD of at least three independent experiments. Deletion of −2576/+66-bp caused a moderate enhancement of luciferase activity, whereas deletions of −352/+66-, −240/+66-, −819/+66-, −145/+66-, and −44/+66-bp caused modest-to-severe decreases in luciferase activity. (B) Mutations at the −145/−44-bp region of the LINC00460 promoter. (C) Luciferase expression is depicted as percent intensity, relative to the expression of the −145/−44-bp construct. All data are presented as the means ± SDs (n = 3). *P < 0.05

    Article Snippet: Various regions of the LINC00460 promoter that were cloned into a pGL3 basic vector (Promega, Madison, WI, USA) expressing the firefly luciferase reporter gene were constructed as described previously [ 25 , 26 ].

    Techniques: Irradiation, Luciferase, Plasmid Preparation, Transfection, Activity Assay, Construct, Expressing