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fopflash tcf reporter construct  (Millipore)


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    Millipore fopflash tcf reporter construct
    Fopflash Tcf Reporter Construct, supplied by Millipore, 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/fopflash+construct/fopflash+tcf+reporter+construct/pm36255661-37-18-22
    Average 90 stars, based on 1 article reviews
    fopflash tcf reporter construct - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Luciferase:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).

    Activity Assay:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).

    Reporter Assay:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).

    Construct:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).

    Sequencing:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).

    Mutagenesis:

    Article Title: CYP24A1 Involvement in Inflammatory Factor Regulation Occurs via the Wnt Signaling Pathway.
    Article Snippet: 1.2 Oligonucleotides The oligonucleotides for gene silencing were chemically synthesized by GenePharma (China) based on the sequence of CYP24A1 and are as follows: CYP24A1 small interfering RNA (siRNA) (siCYP24A1), 5′-CAAACAGUCUAAUGUGGAUTT-3′ (sense), 5′-AUCCACAUUAGACUGUUUGTT-3′ (antisense); siRNA negative control (siNC), 5′-UUCUCCGAACGUGUCACGUTT-3′ (sense), 5′-ACGUGACACGUUCGGAGAATT-3′ (antisense); GAPDH positive control, 5′-UGACCUCAACUACAUGGUUTT-3′ (sense), 5′-AACCAUGUAGUUGAGGUCATT -3′ (antisense). .. 1.3 Luciferase Assay To assay β-catenin/T-cell factor (TCF) activity, a luciferase reporter assay was performed using TOPflash and FOPflash TCF reporter constructs (Millipore, USA), which contained either the TCF/ lymphoid enhancer factor consensus sequence (TOPflash) or the mutant (FOPflash) TCF-binding sites, as described previously[13]. .. The PRL-TK plasmid was from Promega (USA), and DH5α was from Invitrogen (USA).



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    Smurf1 promoted Wnt/β-catenin signaling activation. ( A ) Parental and Smurf1-overexpressing AGS cells were transfected with TOPflash and <t>FOPflash</t> reporters and treated with Wnt3a, respectively. Wnt/β-catenin signaling activation was assessed using the TOPflash/FOPflash dual luciferase reporter system. Relative luciferase units (RLU) were calculated to assess β-catenin-triggered transcription. After <t>Smurf1</t> <t>overexpression</t> in AGS cells, cytoplasmic ( B and D ) and nuclear ( C and D ) β-catenin protein levels were measured using the western blot assay. β-actin and Lamin B1 served as cytoplasmic and nuclear markers, respectively. ( E ) After Smurf1 overexpression in AGS cells, β-catenin nuclear translocation was assessed using IF analysis. Red fluorescence indicated β-catenin, and blue fluorescence indicated the nucleus. The results were shown as the median (1st quartile and 3rd quartile). * p < 0.05, ** p < 0.01.
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    USP2a upregulates β-catenin protein and promotes its transcriptional activity. A. Each SFB-tagged deubiquitinase was co-transfected with MYC-tagged β-catenin into HEK293T cells, followed by pulldown with S-protein beads and immunoblotting with antibodies against FLAG and MYC. B. Either β-catenin-responsive TOPflash or its mutant <t>FOPflash</t> construct was co-transfected with each SFB-tagged deubiquitinase and Renilla luciferase into HEK293T cells. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity. MYC-tagged β-catenin serves as a positive control. Error bars are S.D. C. SFB-tagged GFP, USP2a, USP26, and USP42 were co-transfected with MYC-tagged β-catenin into HEK293T cells, and pulled down with S-protein beads. Antibodies against MYC and FLAG were used to detect β-catenin and DUBs. CypB (cyclophilin B) serves as the loading control. D. Left panel: luciferase reporter assay validating that the 4 candidate deubiquitinases (USP2a, USP36, DUB3, and OTUD7B) promote the transcriptional activity of β-catenin. Error bars are S.D. ***: P < 0.001. Right panel: immunoblotting of HSP90 and SFB-tagged GFP, USP2a, USP36, DUB3, and OTUD7B in HEK293T cells. HSP90 serves as the loading control. T: TOPflash; F: FOPflash. E. Each SFB-tagged candidate deubiquitinase was co-transfected with <t>HA-tagged</t> <t>ubiquitin</t> and MYC-tagged β-catenin into HEK293T cells. After MG132 treatment for 6 hours, β-catenin was immunoprecipitated with a MYC-specific antibody, followed by immunoblotting with antibodies against HA and MYC. F. Immunoblotting of β-catenin, FLAG, and HSP90 in HEK293T cells transfected with SFB-tagged GFP, USP2a, USP36, DUB3, or OTUD7B. G. qPCR of CTNNB1 (the gene that encodes β-catenin) in HEK293T cells transfected with the empty vector, wild-type USP2a, or the catalytically inactive mutant (C276A). Error bars are S.D. n.s.: not significant. H. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNAs. I. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNA with or without ectopic expression of USP2a.
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    Image Search Results


    Smurf1 promoted Wnt/β-catenin signaling activation. ( A ) Parental and Smurf1-overexpressing AGS cells were transfected with TOPflash and FOPflash reporters and treated with Wnt3a, respectively. Wnt/β-catenin signaling activation was assessed using the TOPflash/FOPflash dual luciferase reporter system. Relative luciferase units (RLU) were calculated to assess β-catenin-triggered transcription. After Smurf1 overexpression in AGS cells, cytoplasmic ( B and D ) and nuclear ( C and D ) β-catenin protein levels were measured using the western blot assay. β-actin and Lamin B1 served as cytoplasmic and nuclear markers, respectively. ( E ) After Smurf1 overexpression in AGS cells, β-catenin nuclear translocation was assessed using IF analysis. Red fluorescence indicated β-catenin, and blue fluorescence indicated the nucleus. The results were shown as the median (1st quartile and 3rd quartile). * p < 0.05, ** p < 0.01.

    Journal: Scientific Reports

    Article Title: Smurf1 promotes gastric cancer progression by regulating Axin2-dependent Wnt signaling pathway

    doi: 10.1038/s41598-025-23707-3

    Figure Lengend Snippet: Smurf1 promoted Wnt/β-catenin signaling activation. ( A ) Parental and Smurf1-overexpressing AGS cells were transfected with TOPflash and FOPflash reporters and treated with Wnt3a, respectively. Wnt/β-catenin signaling activation was assessed using the TOPflash/FOPflash dual luciferase reporter system. Relative luciferase units (RLU) were calculated to assess β-catenin-triggered transcription. After Smurf1 overexpression in AGS cells, cytoplasmic ( B and D ) and nuclear ( C and D ) β-catenin protein levels were measured using the western blot assay. β-actin and Lamin B1 served as cytoplasmic and nuclear markers, respectively. ( E ) After Smurf1 overexpression in AGS cells, β-catenin nuclear translocation was assessed using IF analysis. Red fluorescence indicated β-catenin, and blue fluorescence indicated the nucleus. The results were shown as the median (1st quartile and 3rd quartile). * p < 0.05, ** p < 0.01.

    Article Snippet: After Smurf1 overexpression, AGS cells were co-transfected with TOPflash construct (80 ng, Merck) or FOPflash construct (Merck) and pRL-TK plasmid (8 ng, Promega, WI, USA) using PEI max transfection reagent.

    Techniques: Activation Assay, Transfection, Luciferase, Over Expression, Western Blot, Translocation Assay, Fluorescence

    USP2a upregulates β-catenin protein and promotes its transcriptional activity. A. Each SFB-tagged deubiquitinase was co-transfected with MYC-tagged β-catenin into HEK293T cells, followed by pulldown with S-protein beads and immunoblotting with antibodies against FLAG and MYC. B. Either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with each SFB-tagged deubiquitinase and Renilla luciferase into HEK293T cells. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity. MYC-tagged β-catenin serves as a positive control. Error bars are S.D. C. SFB-tagged GFP, USP2a, USP26, and USP42 were co-transfected with MYC-tagged β-catenin into HEK293T cells, and pulled down with S-protein beads. Antibodies against MYC and FLAG were used to detect β-catenin and DUBs. CypB (cyclophilin B) serves as the loading control. D. Left panel: luciferase reporter assay validating that the 4 candidate deubiquitinases (USP2a, USP36, DUB3, and OTUD7B) promote the transcriptional activity of β-catenin. Error bars are S.D. ***: P < 0.001. Right panel: immunoblotting of HSP90 and SFB-tagged GFP, USP2a, USP36, DUB3, and OTUD7B in HEK293T cells. HSP90 serves as the loading control. T: TOPflash; F: FOPflash. E. Each SFB-tagged candidate deubiquitinase was co-transfected with HA-tagged ubiquitin and MYC-tagged β-catenin into HEK293T cells. After MG132 treatment for 6 hours, β-catenin was immunoprecipitated with a MYC-specific antibody, followed by immunoblotting with antibodies against HA and MYC. F. Immunoblotting of β-catenin, FLAG, and HSP90 in HEK293T cells transfected with SFB-tagged GFP, USP2a, USP36, DUB3, or OTUD7B. G. qPCR of CTNNB1 (the gene that encodes β-catenin) in HEK293T cells transfected with the empty vector, wild-type USP2a, or the catalytically inactive mutant (C276A). Error bars are S.D. n.s.: not significant. H. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNAs. I. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNA with or without ectopic expression of USP2a.

    Journal: American Journal of Cancer Research

    Article Title: Ubiquitin-specific peptidase 2a (USP2a) deubiquitinates and stabilizes β-catenin

    doi:

    Figure Lengend Snippet: USP2a upregulates β-catenin protein and promotes its transcriptional activity. A. Each SFB-tagged deubiquitinase was co-transfected with MYC-tagged β-catenin into HEK293T cells, followed by pulldown with S-protein beads and immunoblotting with antibodies against FLAG and MYC. B. Either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with each SFB-tagged deubiquitinase and Renilla luciferase into HEK293T cells. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity. MYC-tagged β-catenin serves as a positive control. Error bars are S.D. C. SFB-tagged GFP, USP2a, USP26, and USP42 were co-transfected with MYC-tagged β-catenin into HEK293T cells, and pulled down with S-protein beads. Antibodies against MYC and FLAG were used to detect β-catenin and DUBs. CypB (cyclophilin B) serves as the loading control. D. Left panel: luciferase reporter assay validating that the 4 candidate deubiquitinases (USP2a, USP36, DUB3, and OTUD7B) promote the transcriptional activity of β-catenin. Error bars are S.D. ***: P < 0.001. Right panel: immunoblotting of HSP90 and SFB-tagged GFP, USP2a, USP36, DUB3, and OTUD7B in HEK293T cells. HSP90 serves as the loading control. T: TOPflash; F: FOPflash. E. Each SFB-tagged candidate deubiquitinase was co-transfected with HA-tagged ubiquitin and MYC-tagged β-catenin into HEK293T cells. After MG132 treatment for 6 hours, β-catenin was immunoprecipitated with a MYC-specific antibody, followed by immunoblotting with antibodies against HA and MYC. F. Immunoblotting of β-catenin, FLAG, and HSP90 in HEK293T cells transfected with SFB-tagged GFP, USP2a, USP36, DUB3, or OTUD7B. G. qPCR of CTNNB1 (the gene that encodes β-catenin) in HEK293T cells transfected with the empty vector, wild-type USP2a, or the catalytically inactive mutant (C276A). Error bars are S.D. n.s.: not significant. H. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNAs. I. Immunoblotting of USP2a, β-catenin, and CypB in BT549 cells transduced with USP2 shRNA with or without ectopic expression of USP2a.

    Article Snippet: HA-ubiquitin, TOPflash, and FOPflash constructs were from Addgene (plasmid number: 17608, 12456, and 12457).

    Techniques: Activity Assay, Transfection, Western Blot, Mutagenesis, Construct, Luciferase, Positive Control, Control, Reporter Assay, Ubiquitin Proteomics, Immunoprecipitation, Plasmid Preparation, Transduction, shRNA, Expressing

    USP2a activates Wnt/β-catenin signaling. A. Immunoblotting of FLAG-USP2a, β-catenin, HSP90 (cytoplasmic marker), and Lamin B1 (nuclear marker) in cytoplasmic and nuclear fractions of HEK293T cells transfected with the empty vector or SFB-USP2a. B. Top panel: either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with SFB-tagged GFP, USP2a, or USP2aC276A and Renilla luciferase into HEK293T cells. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity. Error bars are S.D. **: P < 0.01. Bottom panel: immunoblotting of SFB-USP2a, SFB-USP2aC276A, and CypB in HEK293T cells. T: TOPflash; F: FOPflash. C. Top panel: either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with the SFB vector or SFB-USP2a and Renilla luciferase into HEK293T cells. Cells were treated with DMSO or 3 µM ML364 for 24 hours. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity, and then TOPflash reads were normalized to FOPflash reads. Error bars are S.E.M. *: P < 0.05; **: P < 0.01. Bottom panel: immunoblotting of SFB-USP2a and CypB in HEK293T cells. D: DMSO; M: ML364. D. Human Wnt signaling targets PCR array analysis of HEK293T cells transfected with SFB-USP2a. Gene expression levels in SFB-USP2a-transfected cells were compared to those in empty vector-transfected cells (log2 scale). E. qPCR of BIRC5, CUBN, FGF7, CDON, BTRC, ANTXR1, and IGF2 in HEK293T cells transfected with the empty vector, SFB-USP2a, or SFB-USP2aC276A. Error bars are S.E.M. *: P < 0.05; **: P < 0.01; ***: P < 0.001. F. qPCR of BIRC5, CUBN, FGF7, CDON, BTRC, ANTXR1, and IGF2 in BT549 cells transduced with USP2 shRNAs or a scramble control (Scr). Error bars are S.E.M. *: P < 0.05; **: P < 0.01; ***: P < 0.001; #: not detectable.

    Journal: American Journal of Cancer Research

    Article Title: Ubiquitin-specific peptidase 2a (USP2a) deubiquitinates and stabilizes β-catenin

    doi:

    Figure Lengend Snippet: USP2a activates Wnt/β-catenin signaling. A. Immunoblotting of FLAG-USP2a, β-catenin, HSP90 (cytoplasmic marker), and Lamin B1 (nuclear marker) in cytoplasmic and nuclear fractions of HEK293T cells transfected with the empty vector or SFB-USP2a. B. Top panel: either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with SFB-tagged GFP, USP2a, or USP2aC276A and Renilla luciferase into HEK293T cells. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity. Error bars are S.D. **: P < 0.01. Bottom panel: immunoblotting of SFB-USP2a, SFB-USP2aC276A, and CypB in HEK293T cells. T: TOPflash; F: FOPflash. C. Top panel: either β-catenin-responsive TOPflash or its mutant FOPflash construct was co-transfected with the SFB vector or SFB-USP2a and Renilla luciferase into HEK293T cells. Cells were treated with DMSO or 3 µM ML364 for 24 hours. A dual luciferase assay was used to determine β-catenin activity. Firefly luciferase activity was normalized to Renilla luciferase activity, and then TOPflash reads were normalized to FOPflash reads. Error bars are S.E.M. *: P < 0.05; **: P < 0.01. Bottom panel: immunoblotting of SFB-USP2a and CypB in HEK293T cells. D: DMSO; M: ML364. D. Human Wnt signaling targets PCR array analysis of HEK293T cells transfected with SFB-USP2a. Gene expression levels in SFB-USP2a-transfected cells were compared to those in empty vector-transfected cells (log2 scale). E. qPCR of BIRC5, CUBN, FGF7, CDON, BTRC, ANTXR1, and IGF2 in HEK293T cells transfected with the empty vector, SFB-USP2a, or SFB-USP2aC276A. Error bars are S.E.M. *: P < 0.05; **: P < 0.01; ***: P < 0.001. F. qPCR of BIRC5, CUBN, FGF7, CDON, BTRC, ANTXR1, and IGF2 in BT549 cells transduced with USP2 shRNAs or a scramble control (Scr). Error bars are S.E.M. *: P < 0.05; **: P < 0.01; ***: P < 0.001; #: not detectable.

    Article Snippet: HA-ubiquitin, TOPflash, and FOPflash constructs were from Addgene (plasmid number: 17608, 12456, and 12457).

    Techniques: Western Blot, Marker, Transfection, Plasmid Preparation, Mutagenesis, Construct, Luciferase, Activity Assay, Gene Expression, Transduction, Control