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paper n a plvx tetone puro vector takara bio  (TaKaRa)


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    TaKaRa paper n a plvx tetone puro vector takara bio
    Paper N A Plvx Tetone Puro Vector Takara Bio, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 89 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plvx+tetone+puro/Lenti-X+Tet-One+Inducible+Expression+System/pm42771527-264-30-34
    Average 95 stars, based on 89 article reviews
    paper n a plvx tetone puro vector takara bio - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Expressing:

    Article Title: Coronavirus protein interaction mapping in bat and human cells identifies molecular and genetic switches for immune evasion and replication
    Article Snippet: .. SARS-CoV-2 and RaTG13 reading frames were codon-optimized for mammalian expression and cloned into pLVX-EF1alpha-IRES-Puro (Takara/Clontech) or pLVX-TetOne-Puro (Clontech) including a 5′ Kozak motif with either N-terminal or C-terminal 2XStrep tags using EcoRI and BamHI restriction sites. .. Similarly, human and bat host protein sequences were codon- optimized for Homo sapiens expression and inserted into pcDNA 3.1 vector (Addgene) with a C-terminal Flag-tag using HindIII and BamHI restriction sites.

    Article Title: Angiopoietin–TIE2 feedforward circuit promotes PIK3CA-driven venous malformations
    Article Snippet: For gene orthology conversion between mouse and human, the ‘HOM_MouseHumanSequence’ dataset from the Mouse Genome Database (MGD) of the Jackson Laboratory was used . .. For doxycycline-inducible lentiviral expression of mutant PIKCA H1047R or constitutively nuclear FOXO1 (FOXO1 A3 ) used in Fig. , V5-tagged PIKCA H1047R or FOXO1 A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Article Title: Distinct mechanisms of replication stress induced by oncogenic RAS and cyclin E1 converge on R-loop-dependent fork reversal.
    Article Snippet: The resulting PCR product was digested with NdeI and EcoRI and cloned along with the EcoRI/BspEI fragment of pQE60-yRad52-Tat11-His6 59 in the plasmid pTXB1 (New England Biolabs) to create a bacterial expression vector for RNH1(D210N)-GFP-Tat11-His6 fusion protein. .. Lentiviral vectors for inducible expression of HRASV12 and cyclin E1, respectively, were constructed by PCR amplification of the respective ORF [primers for HRASV12: 5’- GCAGCAGAATTCGCCACCATGACTGAATACAAG-3’ and 5’- GCAGCAGGATCCTCAGGACAGCACACATTTGC-3’; primers for CCNE1: 5’- GCAGCAGAATTCGCCACCATGCCGAGGGAGCGCAGGG-3’ and 5’- GCAGCAGGATCCTCACGCCATTTCCGGCCCGC-3’] and inserting the resulting PCR product into pLVX-TetOne-Puro (Clontech Laboratories, 631849) between EcoRI and BamHI sites. .. RNH1(D210N)-GFP-Tat11-His6 protein was produced in E. coli BL21-CodonPlus (DE3)- RIL (Agilent Technologies, 230245) transformed with the above pTXB1-base vector.

    Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity.
    Article Snippet: .. The fragments were inserted into the BamHI site of the CSII-EF-MCSIRES2-Venus vector (RIKEN BRC) for constitutive overexpression, or into the EcoRI and BamHI sites of pLVX-TetOne-Puro (Clontech, Mountain View, CA, USA) for inducible expression, using the In-Fusion HD Cloning Kit (Clontech). .. CSII-EF-MCS-IRES2-Venus was provided by RIKEN BRC through the National BioResource Project of MEXT (cat. RDB04384).

    Article Title: Angiopoietin-TIE2 feedforward circuit promotes PIK3CA-driven venous malformations.
    Article Snippet: .. For doxycycline-inducible lentiviral expression of mutant PIKCAH1047R or constitutively nuclear FOXO1 (FOXO1A3) used in Fig. 6e, f, V5-tagged PIKCAH1047R or FOXO1A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Clone Assay:

    Article Title: Coronavirus protein interaction mapping in bat and human cells identifies molecular and genetic switches for immune evasion and replication
    Article Snippet: .. SARS-CoV-2 and RaTG13 reading frames were codon-optimized for mammalian expression and cloned into pLVX-EF1alpha-IRES-Puro (Takara/Clontech) or pLVX-TetOne-Puro (Clontech) including a 5′ Kozak motif with either N-terminal or C-terminal 2XStrep tags using EcoRI and BamHI restriction sites. .. Similarly, human and bat host protein sequences were codon- optimized for Homo sapiens expression and inserted into pcDNA 3.1 vector (Addgene) with a C-terminal Flag-tag using HindIII and BamHI restriction sites.

    Article Title: Netrin-1 inhibits the attachment and internalization of Hepatitis B virus for hepatocyte infection
    Article Snippet: Open reading frames of the wild-type and truncated forms of Netrin-1 and LIPG (with the signal sequence retained to ensure proper secretion) were amplified using the Netrin-1 cDNA plasmid (RC218429; OriGene, Rockville, MD) or LIPG cDNA plasmid (RC209248; OriGene) as templates. .. The resulting DNA fragments were cloned into the pLVX-TetOne-Puro or pLVX-TetOne-Hygro vector (Takara Bio USA). .. Dox-inducible stable HepG2-NTCP-YFP cell lines were then generated using the Lenti-X Tet-One Inducible Expression System (Takara Bio USA).

    Article Title: Angiopoietin–TIE2 feedforward circuit promotes PIK3CA-driven venous malformations
    Article Snippet: For gene orthology conversion between mouse and human, the ‘HOM_MouseHumanSequence’ dataset from the Mouse Genome Database (MGD) of the Jackson Laboratory was used . .. For doxycycline-inducible lentiviral expression of mutant PIKCA H1047R or constitutively nuclear FOXO1 (FOXO1 A3 ) used in Fig. , V5-tagged PIKCA H1047R or FOXO1 A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Article Title: Angiopoietin-TIE2 feedforward circuit promotes PIK3CA-driven venous malformations.
    Article Snippet: .. For doxycycline-inducible lentiviral expression of mutant PIKCAH1047R or constitutively nuclear FOXO1 (FOXO1A3) used in Fig. 6e, f, V5-tagged PIKCAH1047R or FOXO1A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Plasmid Preparation:

    Article Title: Netrin-1 inhibits the attachment and internalization of Hepatitis B virus for hepatocyte infection
    Article Snippet: Open reading frames of the wild-type and truncated forms of Netrin-1 and LIPG (with the signal sequence retained to ensure proper secretion) were amplified using the Netrin-1 cDNA plasmid (RC218429; OriGene, Rockville, MD) or LIPG cDNA plasmid (RC209248; OriGene) as templates. .. The resulting DNA fragments were cloned into the pLVX-TetOne-Puro or pLVX-TetOne-Hygro vector (Takara Bio USA). .. Dox-inducible stable HepG2-NTCP-YFP cell lines were then generated using the Lenti-X Tet-One Inducible Expression System (Takara Bio USA).

    Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity.
    Article Snippet: .. The fragments were inserted into the BamHI site of the CSII-EF-MCSIRES2-Venus vector (RIKEN BRC) for constitutive overexpression, or into the EcoRI and BamHI sites of pLVX-TetOne-Puro (Clontech, Mountain View, CA, USA) for inducible expression, using the In-Fusion HD Cloning Kit (Clontech). .. CSII-EF-MCS-IRES2-Venus was provided by RIKEN BRC through the National BioResource Project of MEXT (cat. RDB04384).

    Mutagenesis:

    Article Title: Angiopoietin–TIE2 feedforward circuit promotes PIK3CA-driven venous malformations
    Article Snippet: For gene orthology conversion between mouse and human, the ‘HOM_MouseHumanSequence’ dataset from the Mouse Genome Database (MGD) of the Jackson Laboratory was used . .. For doxycycline-inducible lentiviral expression of mutant PIKCA H1047R or constitutively nuclear FOXO1 (FOXO1 A3 ) used in Fig. , V5-tagged PIKCA H1047R or FOXO1 A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Article Title: Angiopoietin-TIE2 feedforward circuit promotes PIK3CA-driven venous malformations.
    Article Snippet: .. For doxycycline-inducible lentiviral expression of mutant PIKCAH1047R or constitutively nuclear FOXO1 (FOXO1A3) used in Fig. 6e, f, V5-tagged PIKCAH1047R or FOXO1A3 cDNAs were cloned into pLVX-TetOne-Puro (Clontech). .. Lentivirus production was performed by co-transfection of HEK293FT cells with pMD2.G (Addgene, 12259), psPAX2 (Addgene, 12260) and transfer plasmids.

    Construct:

    Article Title: Distinct mechanisms of replication stress induced by oncogenic RAS and cyclin E1 converge on R-loop-dependent fork reversal.
    Article Snippet: The resulting PCR product was digested with NdeI and EcoRI and cloned along with the EcoRI/BspEI fragment of pQE60-yRad52-Tat11-His6 59 in the plasmid pTXB1 (New England Biolabs) to create a bacterial expression vector for RNH1(D210N)-GFP-Tat11-His6 fusion protein. .. Lentiviral vectors for inducible expression of HRASV12 and cyclin E1, respectively, were constructed by PCR amplification of the respective ORF [primers for HRASV12: 5’- GCAGCAGAATTCGCCACCATGACTGAATACAAG-3’ and 5’- GCAGCAGGATCCTCAGGACAGCACACATTTGC-3’; primers for CCNE1: 5’- GCAGCAGAATTCGCCACCATGCCGAGGGAGCGCAGGG-3’ and 5’- GCAGCAGGATCCTCACGCCATTTCCGGCCCGC-3’] and inserting the resulting PCR product into pLVX-TetOne-Puro (Clontech Laboratories, 631849) between EcoRI and BamHI sites. .. RNH1(D210N)-GFP-Tat11-His6 protein was produced in E. coli BL21-CodonPlus (DE3)- RIL (Agilent Technologies, 230245) transformed with the above pTXB1-base vector.

    Polymerase Chain Reaction:

    Article Title: Distinct mechanisms of replication stress induced by oncogenic RAS and cyclin E1 converge on R-loop-dependent fork reversal.
    Article Snippet: The resulting PCR product was digested with NdeI and EcoRI and cloned along with the EcoRI/BspEI fragment of pQE60-yRad52-Tat11-His6 59 in the plasmid pTXB1 (New England Biolabs) to create a bacterial expression vector for RNH1(D210N)-GFP-Tat11-His6 fusion protein. .. Lentiviral vectors for inducible expression of HRASV12 and cyclin E1, respectively, were constructed by PCR amplification of the respective ORF [primers for HRASV12: 5’- GCAGCAGAATTCGCCACCATGACTGAATACAAG-3’ and 5’- GCAGCAGGATCCTCAGGACAGCACACATTTGC-3’; primers for CCNE1: 5’- GCAGCAGAATTCGCCACCATGCCGAGGGAGCGCAGGG-3’ and 5’- GCAGCAGGATCCTCACGCCATTTCCGGCCCGC-3’] and inserting the resulting PCR product into pLVX-TetOne-Puro (Clontech Laboratories, 631849) between EcoRI and BamHI sites. .. RNH1(D210N)-GFP-Tat11-His6 protein was produced in E. coli BL21-CodonPlus (DE3)- RIL (Agilent Technologies, 230245) transformed with the above pTXB1-base vector.

    Amplification:

    Article Title: Distinct mechanisms of replication stress induced by oncogenic RAS and cyclin E1 converge on R-loop-dependent fork reversal.
    Article Snippet: The resulting PCR product was digested with NdeI and EcoRI and cloned along with the EcoRI/BspEI fragment of pQE60-yRad52-Tat11-His6 59 in the plasmid pTXB1 (New England Biolabs) to create a bacterial expression vector for RNH1(D210N)-GFP-Tat11-His6 fusion protein. .. Lentiviral vectors for inducible expression of HRASV12 and cyclin E1, respectively, were constructed by PCR amplification of the respective ORF [primers for HRASV12: 5’- GCAGCAGAATTCGCCACCATGACTGAATACAAG-3’ and 5’- GCAGCAGGATCCTCAGGACAGCACACATTTGC-3’; primers for CCNE1: 5’- GCAGCAGAATTCGCCACCATGCCGAGGGAGCGCAGGG-3’ and 5’- GCAGCAGGATCCTCACGCCATTTCCGGCCCGC-3’] and inserting the resulting PCR product into pLVX-TetOne-Puro (Clontech Laboratories, 631849) between EcoRI and BamHI sites. .. RNH1(D210N)-GFP-Tat11-His6 protein was produced in E. coli BL21-CodonPlus (DE3)- RIL (Agilent Technologies, 230245) transformed with the above pTXB1-base vector.

    Over Expression:

    Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity.
    Article Snippet: .. The fragments were inserted into the BamHI site of the CSII-EF-MCSIRES2-Venus vector (RIKEN BRC) for constitutive overexpression, or into the EcoRI and BamHI sites of pLVX-TetOne-Puro (Clontech, Mountain View, CA, USA) for inducible expression, using the In-Fusion HD Cloning Kit (Clontech). .. CSII-EF-MCS-IRES2-Venus was provided by RIKEN BRC through the National BioResource Project of MEXT (cat. RDB04384).

    Cloning:

    Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity.
    Article Snippet: .. The fragments were inserted into the BamHI site of the CSII-EF-MCSIRES2-Venus vector (RIKEN BRC) for constitutive overexpression, or into the EcoRI and BamHI sites of pLVX-TetOne-Puro (Clontech, Mountain View, CA, USA) for inducible expression, using the In-Fusion HD Cloning Kit (Clontech). .. CSII-EF-MCS-IRES2-Venus was provided by RIKEN BRC through the National BioResource Project of MEXT (cat. RDB04384).



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