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fuw dcas9 tet1cd p2a bfp  (Addgene inc)


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    Addgene inc fuw dcas9 tet1cd p2a bfp
    Fuw Dcas9 Tet1cd P2a Bfp, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fuw+dcas9+tet1cd+plasmid/Fuw-dCas9-Tet1CD-P2A-BFP+(Plasmid+%23108245)/pm41896915-81-8-14
    Average 92 stars, based on 8 article reviews
    fuw dcas9 tet1cd p2a bfp - by Bioz Stars, 2026-09
    92/100 stars

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    Related Articles

    CRISPR:

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy
    Article Snippet: .. The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described. .. This plasmid was obtained from Addgene ( http://www.addgene.org/ ).

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy.
    Article Snippet: .. Plasmid design and construction of CRISPR/dCas9-based epigenetic editing system The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described.69 This plasmid was obtained from Addgene (http://www.addgene.org/). .. Single guide RNA (sgRNA) expression vectors were generated by annealing BARD1 target-specific oligonucleotides and inserting them into the BsmBI restriction site of a modified gRNA backbone (Addgene plasmid #52963).

    Construct:

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy
    Article Snippet: .. The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described. .. This plasmid was obtained from Addgene ( http://www.addgene.org/ ).

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy.
    Article Snippet: .. Plasmid design and construction of CRISPR/dCas9-based epigenetic editing system The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described.69 This plasmid was obtained from Addgene (http://www.addgene.org/). .. Single guide RNA (sgRNA) expression vectors were generated by annealing BARD1 target-specific oligonucleotides and inserting them into the BsmBI restriction site of a modified gRNA backbone (Addgene plasmid #52963).

    Plasmid Preparation:

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy
    Article Snippet: .. The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described. .. This plasmid was obtained from Addgene ( http://www.addgene.org/ ).

    Article Title: Epigenetic modulation of BARD1 to enhance anti-VEGF therapy.
    Article Snippet: .. Plasmid design and construction of CRISPR/dCas9-based epigenetic editing system The CRISPR/dCas9-based epigenetic editing system was constructed using the Fuw-dCas9-Tet1CD plasmid (Addgene plasmid #84475), which encodes a catalytically inactive Cas9 fused to the catalytic domain of Tet1, as previously described.69 This plasmid was obtained from Addgene (http://www.addgene.org/). .. Single guide RNA (sgRNA) expression vectors were generated by annealing BARD1 target-specific oligonucleotides and inserting them into the BsmBI restriction site of a modified gRNA backbone (Addgene plasmid #52963).

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer.
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Article Title: Ten-Eleven Translocation Ablation Impairs Cardiac Differentiation of Mouse Embryonic Stem Cells.
    Article Snippet: Ten-eleven Translocation (TET) dioxygenases mediated DNA methylation oxidation plays an important role in regulating the embryonic stem cells (ESCs) differentiation.. Herein, we utilized a CRISPR/Cas9 based genome editing method to generate single, double, and triple Tet-deficient mouse ESCs (mESCs) and differentiated these cells toward cardiac progenitors.. By using emerald green fluorescent protein (GFP; emGFP) expression under the control of Nkx2.5 promoter as marker for cardiac progenitor cells, we discovered that Tet1 and Tet2 depletion significantly impaired mESC-to-cardiac progenitor differentiation.

    Article Title: Host Cell Transcriptional Tuning with CRISPR/dCas9 to Mitigate the Effects of Toxin Exposure.
    Article Snippet: Anthrax infection is caused byBacillus anthracis, a bacterium that once established within the host releases lethal toxin (LeTx).. Anthrax LeTx is internalized by the capillary morphogenesis protein 2/anthrax toxin receptor 2 (CMG2/ANTXR2) cell surface receptor on mammalian cells.. Once inside the cell, LeTx cleaves mitogen-activated protein kinases (MAPKs), ultimately leading to cell death.

    Amplification:

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer.
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Clone Assay:

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer.
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Cloning:

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Article Title: TERT upstream promoter methylation regulates TERT expression and acts as a therapeutic target in TERT promoter mutation-negative thyroid cancer.
    Article Snippet: .. The Flag-AviTag-dCas9-SV40NLS fragment was amplified from the pEF1a-FB-dCas9-puro plasmid (#100547, Addgene), the 3xSV40NLS-Tet1CD fragment was amplified from the Fuw-dCas9-Tet1CD plasmid (#84475, Addgene), then the two fragments were aligned and cloned into the pCDH-EF1-copGFP-T2A-Puro vector (#72263, Addgene) using the ClonExpress Ultra One Step Cloning Kit (#C115-02, Vazyme Biotech). ..

    Generated:

    Article Title: Host Cell Transcriptional Tuning with CRISPR/dCas9 to Mitigate the Effects of Toxin Exposure.
    Article Snippet: Anthrax infection is caused byBacillus anthracis, a bacterium that once established within the host releases lethal toxin (LeTx).. Anthrax LeTx is internalized by the capillary morphogenesis protein 2/anthrax toxin receptor 2 (CMG2/ANTXR2) cell surface receptor on mammalian cells.. Once inside the cell, LeTx cleaves mitogen-activated protein kinases (MAPKs), ultimately leading to cell death.

    Polymerase Chain Reaction:

    Article Title: Host Cell Transcriptional Tuning with CRISPR/dCas9 to Mitigate the Effects of Toxin Exposure.
    Article Snippet: Anthrax infection is caused byBacillus anthracis, a bacterium that once established within the host releases lethal toxin (LeTx).. Anthrax LeTx is internalized by the capillary morphogenesis protein 2/anthrax toxin receptor 2 (CMG2/ANTXR2) cell surface receptor on mammalian cells.. Once inside the cell, LeTx cleaves mitogen-activated protein kinases (MAPKs), ultimately leading to cell death.

    Sequencing:

    Article Title: Host Cell Transcriptional Tuning with CRISPR/dCas9 to Mitigate the Effects of Toxin Exposure.
    Article Snippet: Anthrax infection is caused byBacillus anthracis, a bacterium that once established within the host releases lethal toxin (LeTx).. Anthrax LeTx is internalized by the capillary morphogenesis protein 2/anthrax toxin receptor 2 (CMG2/ANTXR2) cell surface receptor on mammalian cells.. Once inside the cell, LeTx cleaves mitogen-activated protein kinases (MAPKs), ultimately leading to cell death.



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