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minimal cmv promoter  (Addgene inc)


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    Structured Review

    Addgene inc minimal cmv promoter
    Minimal Cmv Promoter, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/minimal+cmv+promoter/pLenti+CMVtight+eGFP+Puro+(w771-1)+(Plasmid+%2326431)/pmc12802846-169-32-35
    Average 94 stars, based on 14 article reviews
    minimal cmv promoter - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Sequencing:

    Article Title: In Situ synNotch-Programmed Astrocytes Sense and Attenuate Neuronal Apoptosis.
    Article Snippet: The promoters on the 5′-terminal of synNotch receptor genes were a CMV promoter with a CMV enhancer or a GfaABC1D promoter followed by a Promega Chimeric Intron (Addgene plasmid, #100889). .. The response element downstream of the synNotch receptor contained an inducible promoter covering five copies of the Gal4 DBD targeting the UAS (5′-GGAGCACTGTCCTCCGAACG-3′) or seven copies of the TetR targeting the TRE sequence (5′-TCCCTATCAGTGATAGAGA-3′), followed by a minimal CMV promoter (Addgene plasmid, #79126). .. The reporter genes coding mCherry, EGFP, Gluc-IgG1 Fc (Addgene plasmid, #189629), and BDNF-Flag, which is a Flag tag (N’DYKDHDGDYKDHDIDYKDDDDK-C’) directly linked to the C-terminal of mouse BDNF (NM_001048139, Met1-Arg249), were downstream of the inducible promoter.

    Article Title: In Situ synNotch-Programmed Astrocytes Sense and Attenuate Neuronal Apoptosis
    Article Snippet: The promoters on the 5′-terminal of synNotch receptor genes were a CMV promoter with a CMV enhancer or a GfaABC1D promoter followed by a Promega Chimeric Intron (Addgene plasmid, #100889). .. The response element downstream of the synNotch receptor contained an inducible promoter covering five copies of the Gal4 DBD targeting the UAS (5′-GGAGCACTGTCCTCCGAACG-3′) or seven copies of the TetR targeting the TRE sequence (5′-TCCCTATCAGTGATAGAGA-3′), followed by a minimal CMV promoter (Addgene plasmid, #79126). .. The reporter genes coding mCherry, EGFP, Gluc-IgG1 Fc (Addgene plasmid, #189629), and BDNF-Flag, which is a Flag tag (N’-DYKDHDGDYKDHDIDYKDDDDK-C’) directly linked to the C-terminal of mouse BDNF ( NM_001048139 , Met1-Arg249), were downstream of the inducible promoter.

    Plasmid Preparation:

    Article Title: In Situ synNotch-Programmed Astrocytes Sense and Attenuate Neuronal Apoptosis.
    Article Snippet: The promoters on the 5′-terminal of synNotch receptor genes were a CMV promoter with a CMV enhancer or a GfaABC1D promoter followed by a Promega Chimeric Intron (Addgene plasmid, #100889). .. The response element downstream of the synNotch receptor contained an inducible promoter covering five copies of the Gal4 DBD targeting the UAS (5′-GGAGCACTGTCCTCCGAACG-3′) or seven copies of the TetR targeting the TRE sequence (5′-TCCCTATCAGTGATAGAGA-3′), followed by a minimal CMV promoter (Addgene plasmid, #79126). .. The reporter genes coding mCherry, EGFP, Gluc-IgG1 Fc (Addgene plasmid, #189629), and BDNF-Flag, which is a Flag tag (N’DYKDHDGDYKDHDIDYKDDDDK-C’) directly linked to the C-terminal of mouse BDNF (NM_001048139, Met1-Arg249), were downstream of the inducible promoter.

    Article Title: A programmable genetic platform for engineering noninvasive biosensors.
    Article Snippet: All final plasmids were assembled via Gibson assembly and verified by whole- plasmid nanopore sequencing (Plasmidsaurus). .. The genes of interest were amplified using Q5 High- Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline- inducible minimal CMV promoter (Addgene, #26431). .. Cell culture, transfections, and transductions Cell lines were obtained from American Type Cell Culture Collection [U87, Jurkat, PC- 12, MDA- MB- 231, and human embryonic kidney (HEK) 293T] or from Clontech (CHO TetON).

    Article Title: A dual-gene reporter-amplifier architecture for enhancing the sensitivity of molecular MRI by water exchange
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200) and Aqp1 were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: In Situ synNotch-Programmed Astrocytes Sense and Attenuate Neuronal Apoptosis
    Article Snippet: The promoters on the 5′-terminal of synNotch receptor genes were a CMV promoter with a CMV enhancer or a GfaABC1D promoter followed by a Promega Chimeric Intron (Addgene plasmid, #100889). .. The response element downstream of the synNotch receptor contained an inducible promoter covering five copies of the Gal4 DBD targeting the UAS (5′-GGAGCACTGTCCTCCGAACG-3′) or seven copies of the TetR targeting the TRE sequence (5′-TCCCTATCAGTGATAGAGA-3′), followed by a minimal CMV promoter (Addgene plasmid, #79126). .. The reporter genes coding mCherry, EGFP, Gluc-IgG1 Fc (Addgene plasmid, #189629), and BDNF-Flag, which is a Flag tag (N’-DYKDHDGDYKDHDIDYKDDDDK-C’) directly linked to the C-terminal of mouse BDNF ( NM_001048139 , Met1-Arg249), were downstream of the inducible promoter.

    Article Title: A Dual-gene Reporter-amplifier Architecture for Enhancing the Sensitivity of Molecular MRI by Water Exchange.
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200), Aqp1, and Aqp1-FKBP12DD were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A programmable genetic platform for engineering noninvasive biosensors
    Article Snippet: .. The genes of interest were amplified using Q5 High-Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline-inducible minimal CMV promoter (Addgene, #26431). ..

    Amplification:

    Article Title: A programmable genetic platform for engineering noninvasive biosensors.
    Article Snippet: All final plasmids were assembled via Gibson assembly and verified by whole- plasmid nanopore sequencing (Plasmidsaurus). .. The genes of interest were amplified using Q5 High- Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline- inducible minimal CMV promoter (Addgene, #26431). .. Cell culture, transfections, and transductions Cell lines were obtained from American Type Cell Culture Collection [U87, Jurkat, PC- 12, MDA- MB- 231, and human embryonic kidney (HEK) 293T] or from Clontech (CHO TetON).

    Article Title: Engineering ligand stabilized aquaporin reporters for magnetic resonance imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences - DHFR (Addgene 29326), ER (Addgene 37261), miniIAA7 (Addgene 129721), SMASh (Addgene 68853), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2X Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N-terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..

    Article Title: A dual-gene reporter-amplifier architecture for enhancing the sensitivity of molecular MRI by water exchange
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200) and Aqp1 were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A Dual-gene Reporter-amplifier Architecture for Enhancing the Sensitivity of Molecular MRI by Water Exchange.
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200), Aqp1, and Aqp1-FKBP12DD were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A programmable genetic platform for engineering noninvasive biosensors
    Article Snippet: .. The genes of interest were amplified using Q5 High-Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline-inducible minimal CMV promoter (Addgene, #26431). ..

    Article Title: Destabilized reporters for background-subtracted, chemically-gated, and multiplexed deep-tissue imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences – DHFR-DD (Addgene 29326), ER-DD (Addgene 37261), miniIAA7 (Addgene 129721), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2× Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N -terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..

    Clone Assay:

    Article Title: A programmable genetic platform for engineering noninvasive biosensors.
    Article Snippet: All final plasmids were assembled via Gibson assembly and verified by whole- plasmid nanopore sequencing (Plasmidsaurus). .. The genes of interest were amplified using Q5 High- Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline- inducible minimal CMV promoter (Addgene, #26431). .. Cell culture, transfections, and transductions Cell lines were obtained from American Type Cell Culture Collection [U87, Jurkat, PC- 12, MDA- MB- 231, and human embryonic kidney (HEK) 293T] or from Clontech (CHO TetON).

    Article Title: Engineering ligand stabilized aquaporin reporters for magnetic resonance imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences - DHFR (Addgene 29326), ER (Addgene 37261), miniIAA7 (Addgene 129721), SMASh (Addgene 68853), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2X Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N-terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..

    Article Title: A dual-gene reporter-amplifier architecture for enhancing the sensitivity of molecular MRI by water exchange
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200) and Aqp1 were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A Dual-gene Reporter-amplifier Architecture for Enhancing the Sensitivity of Molecular MRI by Water Exchange.
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200), Aqp1, and Aqp1-FKBP12DD were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A programmable genetic platform for engineering noninvasive biosensors
    Article Snippet: .. The genes of interest were amplified using Q5 High-Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline-inducible minimal CMV promoter (Addgene, #26431). ..

    Article Title: Destabilized reporters for background-subtracted, chemically-gated, and multiplexed deep-tissue imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences – DHFR-DD (Addgene 29326), ER-DD (Addgene 37261), miniIAA7 (Addgene 129721), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2× Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N -terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..

    Control:

    Article Title: A programmable genetic platform for engineering noninvasive biosensors.
    Article Snippet: All final plasmids were assembled via Gibson assembly and verified by whole- plasmid nanopore sequencing (Plasmidsaurus). .. The genes of interest were amplified using Q5 High- Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline- inducible minimal CMV promoter (Addgene, #26431). .. Cell culture, transfections, and transductions Cell lines were obtained from American Type Cell Culture Collection [U87, Jurkat, PC- 12, MDA- MB- 231, and human embryonic kidney (HEK) 293T] or from Clontech (CHO TetON).

    Article Title: Engineering ligand stabilized aquaporin reporters for magnetic resonance imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences - DHFR (Addgene 29326), ER (Addgene 37261), miniIAA7 (Addgene 129721), SMASh (Addgene 68853), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2X Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N-terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..

    Article Title: A dual-gene reporter-amplifier architecture for enhancing the sensitivity of molecular MRI by water exchange
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200) and Aqp1 were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A Dual-gene Reporter-amplifier Architecture for Enhancing the Sensitivity of Molecular MRI by Water Exchange.
    Article Snippet: .. The DNA sequences encoding Oatp1b3 (Addgene plasmid #132200), Aqp1, and Aqp1-FKBP12DD were amplified using Q5® High-Fidelity 2X Master Mix (New England Biolabs, Ipswich, MA, USA) and cloned by Gibson assembly in a lentiviral transfer vector under the control of a constitutive promoter, EF1α (Addgene plasmid #60058) or a doxycycline-inducible minimal CMV promoter (Addgene plasmid #26431). ..

    Article Title: A programmable genetic platform for engineering noninvasive biosensors
    Article Snippet: .. The genes of interest were amplified using Q5 High-Fidelity DNA Polymerase and cloned into a lentiviral transfer plasmid under the control of either a constitutive promoter EF1α (Addgene, #60058) or a doxycycline-inducible minimal CMV promoter (Addgene, #26431). ..

    Article Title: Destabilized reporters for background-subtracted, chemically-gated, and multiplexed deep-tissue imaging
    Article Snippet: Type F immersion oil was purchased from Leica Microsystems (Deerfield, IL, USA). .. Plasmids harboring the various degron sequences – DHFR-DD (Addgene 29326), ER-DD (Addgene 37261), miniIAA7 (Addgene 129721), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2× Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N -terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431). ..



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    Biochemically-gated imaging of transcriptional activity. (a) Gated reporters leverage genetic AND logic to generate an output only when transcriptional activity ( T x ) is accompanied by an externally added drug (in this case, shield-1). (b) <t>Doxycycline-dependent</t> change in diffusivities of CHO cells expressing conventional DD-free Aqp1 under the control of a doxycycline-inducible minimal CMV promoter. (c) Doxycycline-driven changes in diffusivities of CHO cells expressing Aqp1-FKBP12-DD under the control of a doxycycline-inducible minimal CMV promoter following incubation with shield-1, doxycycline, and both ligands. (d) Representative difference image showing shield-1 gated imaging of transcriptional activity. The difference image was obtained through voxel-wise subtraction of diffusion-weighted datasets (effective b -value ∼1.6 ms μm −2 ) acquired in the presence of shield-1, doxycycline, or both from a dataset acquired in their absence. The resulting image was subsequently denoised using a median filter and presented as a pseudo-colored “hotspot.” Error bars represent the standard deviation ( n = 3–6). *** denotes P < 0.001. P -values were computed based on 2-sided, unpaired t -test (2b) or using one-way ANOVA followed by Tukey's HSD test (2c).
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    Image Search Results


    Biochemically-gated imaging of transcriptional activity. (a) Gated reporters leverage genetic AND logic to generate an output only when transcriptional activity ( T x ) is accompanied by an externally added drug (in this case, shield-1). (b) Doxycycline-dependent change in diffusivities of CHO cells expressing conventional DD-free Aqp1 under the control of a doxycycline-inducible minimal CMV promoter. (c) Doxycycline-driven changes in diffusivities of CHO cells expressing Aqp1-FKBP12-DD under the control of a doxycycline-inducible minimal CMV promoter following incubation with shield-1, doxycycline, and both ligands. (d) Representative difference image showing shield-1 gated imaging of transcriptional activity. The difference image was obtained through voxel-wise subtraction of diffusion-weighted datasets (effective b -value ∼1.6 ms μm −2 ) acquired in the presence of shield-1, doxycycline, or both from a dataset acquired in their absence. The resulting image was subsequently denoised using a median filter and presented as a pseudo-colored “hotspot.” Error bars represent the standard deviation ( n = 3–6). *** denotes P < 0.001. P -values were computed based on 2-sided, unpaired t -test (2b) or using one-way ANOVA followed by Tukey's HSD test (2c).

    Journal: Chemical Science

    Article Title: Destabilized reporters for background-subtracted, chemically-gated, and multiplexed deep-tissue imaging †

    doi: 10.1039/d4sc00377b

    Figure Lengend Snippet: Biochemically-gated imaging of transcriptional activity. (a) Gated reporters leverage genetic AND logic to generate an output only when transcriptional activity ( T x ) is accompanied by an externally added drug (in this case, shield-1). (b) Doxycycline-dependent change in diffusivities of CHO cells expressing conventional DD-free Aqp1 under the control of a doxycycline-inducible minimal CMV promoter. (c) Doxycycline-driven changes in diffusivities of CHO cells expressing Aqp1-FKBP12-DD under the control of a doxycycline-inducible minimal CMV promoter following incubation with shield-1, doxycycline, and both ligands. (d) Representative difference image showing shield-1 gated imaging of transcriptional activity. The difference image was obtained through voxel-wise subtraction of diffusion-weighted datasets (effective b -value ∼1.6 ms μm −2 ) acquired in the presence of shield-1, doxycycline, or both from a dataset acquired in their absence. The resulting image was subsequently denoised using a median filter and presented as a pseudo-colored “hotspot.” Error bars represent the standard deviation ( n = 3–6). *** denotes P < 0.001. P -values were computed based on 2-sided, unpaired t -test (2b) or using one-way ANOVA followed by Tukey's HSD test (2c).

    Article Snippet: Plasmids harboring the various degron sequences – DHFR-DD (Addgene 29326), ER-DD (Addgene 37261), miniIAA7 (Addgene 129721), and FKBP12 (Addgene 17416) were amplified using Q5 High-Fidelity 2× Master Mix and cloned by Gibson assembly in a lentiviral transfer vector at the C or N -terminus of the aquaporin-1 reporter (Aqp1) under the control of either a constitutive promoter, EF1α (Addgene 60058) or a doxycycline-inducible minimal CMV promoter (Addgene 26431).

    Techniques: Imaging, Activity Assay, Expressing, Control, Incubation, Diffusion-based Assay, Standard Deviation