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plvx puro vector  (TaKaRa)


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    Structured Review

    TaKaRa plvx puro vector
    Plvx Puro Vector, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 3518 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plvx+vector/Puromycin/pmc13066983-69-1-3
    Average 96 stars, based on 3518 article reviews
    plvx puro vector - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Isolation:

    Article Title: 2,6-Diaminopurine Induces ACTN3 Premature Termination Codon Readthrough.
    Article Snippet: The ACTN3 gene encodes a sarcomeric α-actinin-3 protein, which forms an antiparallel dimer and constitutes the Z-lines in human skeletal muscle fast-twitch fibers.. In human ACTN3, a nonsense mutation that replaces a CGA codon for the 577th arginine (R) residue with a TGA premature termination codon (PTC; specified as X) produces the R577X polymorphism.. Since ACTN3 577X mRNA is targeted and degraded by a cellular nonsense-mediated mRNA decay (NMD) system, individuals with the homozygous ACTN3 577XX genotype do not express α-actinin-3 protein in the muscles, resulting in a decrease in speed-oriented athletic performance and muscle mass.

    Plasmid Preparation:

    Article Title: 2,6-Diaminopurine Induces ACTN3 Premature Termination Codon Readthrough.
    Article Snippet: The ACTN3 gene encodes a sarcomeric α-actinin-3 protein, which forms an antiparallel dimer and constitutes the Z-lines in human skeletal muscle fast-twitch fibers.. In human ACTN3, a nonsense mutation that replaces a CGA codon for the 577th arginine (R) residue with a TGA premature termination codon (PTC; specified as X) produces the R577X polymorphism.. Since ACTN3 577X mRNA is targeted and degraded by a cellular nonsense-mediated mRNA decay (NMD) system, individuals with the homozygous ACTN3 577XX genotype do not express α-actinin-3 protein in the muscles, resulting in a decrease in speed-oriented athletic performance and muscle mass.

    Article Title: Dolichol biosynthesis in yeast traces the expanded reaction pathway of higher eukaryotes
    Article Snippet: The quantification was performed by Agilent MassHunter Quantitative Analysis software (Agilent Technologies, CA, USA). .. Recombinant lentiviruses were produced in HEK293T cells as previously described using the vectors pUB81 TDA5. pUB81 is a lentiviral expression vector based on the pLVX-PURO (Clontech) plasmid containing EF-1α promoter. ..

    Article Title: TRF2–RAP1 inhibits homology-directed repair of telomeres by promoting BLM-mediated removal of telomere R-loops
    Article Snippet: .. The 3′-UTR shBLM with target sequence 5′- GAATCTCAATGTACATAGA −3′ was cloned into the pSUPER.retro.puro vector (Clontech) and transfected into 293T cells by LipoD293 (SignaGen) to generate shBLM retroviral supernatants. .. The deproteinized reaction mixtures by SDS and proteinase K were passed through Micro Bio-Spin 6 Column (Bio-Rad), equilibrated with buffer B. TRF2–RAP1 (50 nM) was pre-incubated with the D/R-loop substrate (2.5 nM) on ice for 10 min. Then BLM (20–80 nM) was added and incubated at 37°C for 20 min.

    Article Title: Bisphenol A Drives Thyroid Carcinogenesis Through Oxidative Stress-Lipid Metabolic Reprogramming via the PTEN/PI3K/AKT Axis: Therapeutic Reversal by a Curcumin-Modified Quercetin Nanomicelle System.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Article Title: TBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.
    Article Snippet: Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA). .. To establish stable lines expressing Dox-inducible hTDP-43 (WT or 6M)-3×FLAG, pTRE-Tight-hTDP-43 (WT or 6M)3×FLAG-SV40-PuroR was generated by subcloning cDNAs encoding hTDP-43 (WT or 6M)-3×FLAG and the SV40 early promoter–puromycin resistance gene–polyadenylation signal sequence from the pPur vector (#631601, Takara Bio) into the pTRE-Tight vector (#631059, Takara Bio). .. Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA).

    Sequencing:

    Article Title: CDC6/THBS1 accelerates pancreatic cancer progression via AKT-mediated glycolytic reprogramming.
    Article Snippet: For knockdown experiments, shRNA sequences were cloned into pLVX-EGFP lentiviral vectors (Clontech) using AgeI/EcoRI restriction sites. .. The CDC6 coding sequence (NCBI accession: NM_001254) and THBS1 coding sequence (NCBI accession: NM_003246.2)were synthesized and subcloned into pLVX-Puro overexpression vectors (Takara Bio) for ectopic expression. ..

    Article Title: TRF2–RAP1 inhibits homology-directed repair of telomeres by promoting BLM-mediated removal of telomere R-loops
    Article Snippet: .. The 3′-UTR shBLM with target sequence 5′- GAATCTCAATGTACATAGA −3′ was cloned into the pSUPER.retro.puro vector (Clontech) and transfected into 293T cells by LipoD293 (SignaGen) to generate shBLM retroviral supernatants. .. The deproteinized reaction mixtures by SDS and proteinase K were passed through Micro Bio-Spin 6 Column (Bio-Rad), equilibrated with buffer B. TRF2–RAP1 (50 nM) was pre-incubated with the D/R-loop substrate (2.5 nM) on ice for 10 min. Then BLM (20–80 nM) was added and incubated at 37°C for 20 min.

    Article Title: TBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.
    Article Snippet: Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA). .. To establish stable lines expressing Dox-inducible hTDP-43 (WT or 6M)-3×FLAG, pTRE-Tight-hTDP-43 (WT or 6M)3×FLAG-SV40-PuroR was generated by subcloning cDNAs encoding hTDP-43 (WT or 6M)-3×FLAG and the SV40 early promoter–puromycin resistance gene–polyadenylation signal sequence from the pPur vector (#631601, Takara Bio) into the pTRE-Tight vector (#631059, Takara Bio). .. Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA).

    Synthesized:

    Article Title: CDC6/THBS1 accelerates pancreatic cancer progression via AKT-mediated glycolytic reprogramming.
    Article Snippet: For knockdown experiments, shRNA sequences were cloned into pLVX-EGFP lentiviral vectors (Clontech) using AgeI/EcoRI restriction sites. .. The CDC6 coding sequence (NCBI accession: NM_001254) and THBS1 coding sequence (NCBI accession: NM_003246.2)were synthesized and subcloned into pLVX-Puro overexpression vectors (Takara Bio) for ectopic expression. ..

    Over Expression:

    Article Title: CDC6/THBS1 accelerates pancreatic cancer progression via AKT-mediated glycolytic reprogramming.
    Article Snippet: For knockdown experiments, shRNA sequences were cloned into pLVX-EGFP lentiviral vectors (Clontech) using AgeI/EcoRI restriction sites. .. The CDC6 coding sequence (NCBI accession: NM_001254) and THBS1 coding sequence (NCBI accession: NM_003246.2)were synthesized and subcloned into pLVX-Puro overexpression vectors (Takara Bio) for ectopic expression. ..

    Expressing:

    Article Title: CDC6/THBS1 accelerates pancreatic cancer progression via AKT-mediated glycolytic reprogramming.
    Article Snippet: For knockdown experiments, shRNA sequences were cloned into pLVX-EGFP lentiviral vectors (Clontech) using AgeI/EcoRI restriction sites. .. The CDC6 coding sequence (NCBI accession: NM_001254) and THBS1 coding sequence (NCBI accession: NM_003246.2)were synthesized and subcloned into pLVX-Puro overexpression vectors (Takara Bio) for ectopic expression. ..

    Article Title: Dolichol biosynthesis in yeast traces the expanded reaction pathway of higher eukaryotes
    Article Snippet: The quantification was performed by Agilent MassHunter Quantitative Analysis software (Agilent Technologies, CA, USA). .. Recombinant lentiviruses were produced in HEK293T cells as previously described using the vectors pUB81 TDA5. pUB81 is a lentiviral expression vector based on the pLVX-PURO (Clontech) plasmid containing EF-1α promoter. ..

    Article Title: TBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.
    Article Snippet: Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA). .. To establish stable lines expressing Dox-inducible hTDP-43 (WT or 6M)-3×FLAG, pTRE-Tight-hTDP-43 (WT or 6M)3×FLAG-SV40-PuroR was generated by subcloning cDNAs encoding hTDP-43 (WT or 6M)-3×FLAG and the SV40 early promoter–puromycin resistance gene–polyadenylation signal sequence from the pPur vector (#631601, Takara Bio) into the pTRE-Tight vector (#631059, Takara Bio). .. Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA).

    Recombinant:

    Article Title: Dolichol biosynthesis in yeast traces the expanded reaction pathway of higher eukaryotes
    Article Snippet: The quantification was performed by Agilent MassHunter Quantitative Analysis software (Agilent Technologies, CA, USA). .. Recombinant lentiviruses were produced in HEK293T cells as previously described using the vectors pUB81 TDA5. pUB81 is a lentiviral expression vector based on the pLVX-PURO (Clontech) plasmid containing EF-1α promoter. ..

    Produced:

    Article Title: Dolichol biosynthesis in yeast traces the expanded reaction pathway of higher eukaryotes
    Article Snippet: The quantification was performed by Agilent MassHunter Quantitative Analysis software (Agilent Technologies, CA, USA). .. Recombinant lentiviruses were produced in HEK293T cells as previously described using the vectors pUB81 TDA5. pUB81 is a lentiviral expression vector based on the pLVX-PURO (Clontech) plasmid containing EF-1α promoter. ..

    Clone Assay:

    Article Title: TRF2–RAP1 inhibits homology-directed repair of telomeres by promoting BLM-mediated removal of telomere R-loops
    Article Snippet: .. The 3′-UTR shBLM with target sequence 5′- GAATCTCAATGTACATAGA −3′ was cloned into the pSUPER.retro.puro vector (Clontech) and transfected into 293T cells by LipoD293 (SignaGen) to generate shBLM retroviral supernatants. .. The deproteinized reaction mixtures by SDS and proteinase K were passed through Micro Bio-Spin 6 Column (Bio-Rad), equilibrated with buffer B. TRF2–RAP1 (50 nM) was pre-incubated with the D/R-loop substrate (2.5 nM) on ice for 10 min. Then BLM (20–80 nM) was added and incubated at 37°C for 20 min.

    Transfection:

    Article Title: TRF2–RAP1 inhibits homology-directed repair of telomeres by promoting BLM-mediated removal of telomere R-loops
    Article Snippet: .. The 3′-UTR shBLM with target sequence 5′- GAATCTCAATGTACATAGA −3′ was cloned into the pSUPER.retro.puro vector (Clontech) and transfected into 293T cells by LipoD293 (SignaGen) to generate shBLM retroviral supernatants. .. The deproteinized reaction mixtures by SDS and proteinase K were passed through Micro Bio-Spin 6 Column (Bio-Rad), equilibrated with buffer B. TRF2–RAP1 (50 nM) was pre-incubated with the D/R-loop substrate (2.5 nM) on ice for 10 min. Then BLM (20–80 nM) was added and incubated at 37°C for 20 min.

    Article Title: PINK1/Parkin-dependent mitophagy mediates astrocytic inflammatory responses to mitochondrial damage
    Article Snippet: Thawed cells were cultured on plates coated with Growth Factor Reduced Matrigel (Corning) and fed daily with Essential 8 media (Thermo Fisher Scientific). .. After 72h, transfected iPSCs were selected for 48h with 0.5 μg/ml puromycin (Takara). .. Differentiation into iNeurons was performed using an established protocol , in which iPSCs were passaged using Accutase (Sigma-Aldrich) and plated on Matrigel-coated dishes in Induction Media (DMEM/F12 supplemented with 1% N2-supplement [Gibco], 1% NEAA [Gibco], 1% GlutaMAX [Gibco], and 2 μg/ml doxycycline).

    Retroviral:

    Article Title: TRF2–RAP1 inhibits homology-directed repair of telomeres by promoting BLM-mediated removal of telomere R-loops
    Article Snippet: .. The 3′-UTR shBLM with target sequence 5′- GAATCTCAATGTACATAGA −3′ was cloned into the pSUPER.retro.puro vector (Clontech) and transfected into 293T cells by LipoD293 (SignaGen) to generate shBLM retroviral supernatants. .. The deproteinized reaction mixtures by SDS and proteinase K were passed through Micro Bio-Spin 6 Column (Bio-Rad), equilibrated with buffer B. TRF2–RAP1 (50 nM) was pre-incubated with the D/R-loop substrate (2.5 nM) on ice for 10 min. Then BLM (20–80 nM) was added and incubated at 37°C for 20 min.

    Electroporation:

    Article Title: Modeling interregional propagation of α-synuclein in human striatal–midbrain assembloids
    Article Snippet: .. Two days after electroporation, the medium was supplemented with 0.5 μg/mL puromycin (Takara Bio Inc.) for positive selection. ..

    Selection:

    Article Title: Modeling interregional propagation of α-synuclein in human striatal–midbrain assembloids
    Article Snippet: .. Two days after electroporation, the medium was supplemented with 0.5 μg/mL puromycin (Takara Bio Inc.) for positive selection. ..

    Cloning:

    Article Title: Bisphenol A Drives Thyroid Carcinogenesis Through Oxidative Stress-Lipid Metabolic Reprogramming via the PTEN/PI3K/AKT Axis: Therapeutic Reversal by a Curcumin-Modified Quercetin Nanomicelle System.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Introduce:

    Article Title: Bisphenol A Drives Thyroid Carcinogenesis Through Oxidative Stress-Lipid Metabolic Reprogramming via the PTEN/PI3K/AKT Axis: Therapeutic Reversal by a Curcumin-Modified Quercetin Nanomicelle System.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Generated:

    Article Title: TBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.
    Article Snippet: Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA). .. To establish stable lines expressing Dox-inducible hTDP-43 (WT or 6M)-3×FLAG, pTRE-Tight-hTDP-43 (WT or 6M)3×FLAG-SV40-PuroR was generated by subcloning cDNAs encoding hTDP-43 (WT or 6M)-3×FLAG and the SV40 early promoter–puromycin resistance gene–polyadenylation signal sequence from the pPur vector (#631601, Takara Bio) into the pTRE-Tight vector (#631059, Takara Bio). .. Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA).

    Subcloning:

    Article Title: TBK1 eliminates aggregation-prone monomeric TDP-43 through an IFNβ-immunoproteasome pathway in ALS models.
    Article Snippet: Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA). .. To establish stable lines expressing Dox-inducible hTDP-43 (WT or 6M)-3×FLAG, pTRE-Tight-hTDP-43 (WT or 6M)3×FLAG-SV40-PuroR was generated by subcloning cDNAs encoding hTDP-43 (WT or 6M)-3×FLAG and the SV40 early promoter–puromycin resistance gene–polyadenylation signal sequence from the pPur vector (#631601, Takara Bio) into the pTRE-Tight vector (#631059, Takara Bio). .. Predesigned 27mer Dicer-substrate short interfering RNAs (siRNAs) specific for Sting, Irf3, and Ifnb1, and a negative control siRNA were purchased from Integrated DNA Technologies (IDT) (Coralville, IA, USA).



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