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puromycin selection cassette  (Addgene inc)


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    Structured Review

    Addgene inc puromycin selection cassette
    Puromycin Selection Cassette, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 6093 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/puromycin+selection+cassette/lentiCRISPR+v2+(Plasmid+%2352961)/bio_rxiv__64898__2026__03__27__714809-166-38-41
    Average 96 stars, based on 6093 article reviews
    puromycin selection cassette - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Selection:

    Article Title: Mouse neural tube organoids self-organize floorplate through BMP-mediated cluster competition.
    Article Snippet: Primary antibodies used: rabbit anti-FOXA2 (Cell Signalling Technologies, #8186S, 1:1000), andmouse anti-ß-tubulin (MPI-CBG antibody facility, 1:200), HRPconjugated secondary antibodies used: Invitrogen Goat anti-Rabbit/Mouse 1:2000. .. H2A-mCherry was integrated into the Rosa26 safe harbour locus of FOXA2-Venus cell line.We first obtained aRosa26 targeting vector with Puromycin selection cassette (pR26CAGAsiSI/MluI, Addgene 74286, Ralf Kuehn lab, 53), linearised the vector with SwaI restriction digest, and used Gibson Assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST. .. H2A-mCherry was integrated into the Rosa26 safe harbour locus of FOXA2-Venus cell line.We first obtained aRosa26 targeting vector with Puromycin selection cassette (pR26CAGAsiSI/MluI, Addgene 74286, Ralf Kuehn lab, 53), linearised the vector with SwaI restriction digest, and used Gibson Assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST.

    Article Title: Clonal neural tube organoids self-organise floorplate through BMP-mediated cluster competition
    Article Snippet: .. We first obtained a Rosa26 targeting vector with Puromycin selection cassette (pR26 CAG AsiSI/MluI, Addgene 74286, Ralf Kuehn lab, , linearized the vector with SwaI restriction digest, and used Gibson assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST. ..

    Article Title: Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach.
    Article Snippet: Cells were selected with puromycin (1 ng/μl, Sigma) for 3 days, starting at day 2 after transfection. .. The puromycin selection cassette was subsequently excised by transient transfection of a CRE recombinase expression plasmid pCAG-Cre (Addgene 13,775, [94]). ..

    Article Title: The MEMIC is an ex vivo system to model the complexity of the tumor microenvironment
    Article Snippet: To create a hypoxia reporter for live imaging, an existing GFP-based HIF1ɑ reporter (Addgene, 46926 ; ) was subcloned into a lentiviral delivery plasmid using a Gibson assembly-based modular assembly platform (GMAP) ( ). .. The 5xHRE-GFP region and a PGK-driven puromycin selection cassette from the pMSCV-Peredox-mCherry-NLS plasmid (Addgene, 32385 ) were amplified using primers containing overhangs with the homology sites for GMAP cloning and inserted into a lentiviral vector (LV 1-5; Addgene, 68411 ). ..

    Article Title: Complementary constraints in germ and immune cells shape evolution of gene regulation and phenotype
    Article Snippet: .. sgRNAs were designed to target the NGG sites nearest to and flanking the identified CTCF binding domain within the swapped human promoter sequence ( Table S6 ). sgRNAs were cloned into lentiCRISPR v2 plasmid with a Cas9 and puromycin selection cassette (Addgene, 52961; RRID: Addgene_52961) as previously described , . .. Briefly, plasmid was digested with BsmBI-v2 (NEB, R0580) at 55°C for 1 hour.

    Article Title: Targeting leucine-rich repeat kinase 2 overcomes resistance to oncolytic herpes simplex virus-based therapies in glioblastoma.
    Article Snippet: .. The gene encoding human NECTIN1 was synthesized by GENEWIZ and cloned into the LentiCRISPRv2GFP vector, which contains a puromycin selection cassette (Addgene, 82416). .. Constructs expressing human NECTIN1, full-length (FL) LRRK2, truncated LRRK2, FL STAT1, truncated STAT1, and TBK1 were synthesized by GENEWIZ.

    Article Title: Supporting Information for Liver cancer development driven by the AP-1/c-Jun~Fra-2 dimer through c- Myc
    Article Snippet: .. To delete the c-MYC (WRE) enhancer, two flanking CRISPR guides were designed (sg_1: GCCCCTTTGTGGCCTAGGGC and sg_2: GCCCTAGGCCACAAAGGGGC) and cloned into the lentiCRISPR v2 backbone containing a puromycin selection cassette (Addgene#52961) and the resulting plasmid transfected in HepG2 cells using Xtreme gene (Sigma). ..

    Sequencing:

    Article Title: Mouse neural tube organoids self-organize floorplate through BMP-mediated cluster competition.
    Article Snippet: Primary antibodies used: rabbit anti-FOXA2 (Cell Signalling Technologies, #8186S, 1:1000), andmouse anti-ß-tubulin (MPI-CBG antibody facility, 1:200), HRPconjugated secondary antibodies used: Invitrogen Goat anti-Rabbit/Mouse 1:2000. .. H2A-mCherry was integrated into the Rosa26 safe harbour locus of FOXA2-Venus cell line.We first obtained aRosa26 targeting vector with Puromycin selection cassette (pR26CAGAsiSI/MluI, Addgene 74286, Ralf Kuehn lab, 53), linearised the vector with SwaI restriction digest, and used Gibson Assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST. .. H2A-mCherry was integrated into the Rosa26 safe harbour locus of FOXA2-Venus cell line.We first obtained aRosa26 targeting vector with Puromycin selection cassette (pR26CAGAsiSI/MluI, Addgene 74286, Ralf Kuehn lab, 53), linearised the vector with SwaI restriction digest, and used Gibson Assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST.

    Article Title: Clonal neural tube organoids self-organise floorplate through BMP-mediated cluster competition
    Article Snippet: .. We first obtained a Rosa26 targeting vector with Puromycin selection cassette (pR26 CAG AsiSI/MluI, Addgene 74286, Ralf Kuehn lab, , linearized the vector with SwaI restriction digest, and used Gibson assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST. ..

    Article Title: Complementary constraints in germ and immune cells shape evolution of gene regulation and phenotype
    Article Snippet: .. sgRNAs were designed to target the NGG sites nearest to and flanking the identified CTCF binding domain within the swapped human promoter sequence ( Table S6 ). sgRNAs were cloned into lentiCRISPR v2 plasmid with a Cas9 and puromycin selection cassette (Addgene, 52961; RRID: Addgene_52961) as previously described , . .. Briefly, plasmid was digested with BsmBI-v2 (NEB, R0580) at 55°C for 1 hour.

    Plasmid Preparation:

    Article Title: Clonal neural tube organoids self-organise floorplate through BMP-mediated cluster competition
    Article Snippet: .. We first obtained a Rosa26 targeting vector with Puromycin selection cassette (pR26 CAG AsiSI/MluI, Addgene 74286, Ralf Kuehn lab, , linearized the vector with SwaI restriction digest, and used Gibson assembly to insert the Gateway destination sequence immediately 3’ to the splice acceptor site, and created a new vector termed pR26-sA-DEST. ..

    Article Title: Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach.
    Article Snippet: Cells were selected with puromycin (1 ng/μl, Sigma) for 3 days, starting at day 2 after transfection. .. The puromycin selection cassette was subsequently excised by transient transfection of a CRE recombinase expression plasmid pCAG-Cre (Addgene 13,775, [94]). ..

    Article Title: The MEMIC is an ex vivo system to model the complexity of the tumor microenvironment
    Article Snippet: To create a hypoxia reporter for live imaging, an existing GFP-based HIF1ɑ reporter (Addgene, 46926 ; ) was subcloned into a lentiviral delivery plasmid using a Gibson assembly-based modular assembly platform (GMAP) ( ). .. The 5xHRE-GFP region and a PGK-driven puromycin selection cassette from the pMSCV-Peredox-mCherry-NLS plasmid (Addgene, 32385 ) were amplified using primers containing overhangs with the homology sites for GMAP cloning and inserted into a lentiviral vector (LV 1-5; Addgene, 68411 ). ..

    Article Title: Complementary constraints in germ and immune cells shape evolution of gene regulation and phenotype
    Article Snippet: .. sgRNAs were designed to target the NGG sites nearest to and flanking the identified CTCF binding domain within the swapped human promoter sequence ( Table S6 ). sgRNAs were cloned into lentiCRISPR v2 plasmid with a Cas9 and puromycin selection cassette (Addgene, 52961; RRID: Addgene_52961) as previously described , . .. Briefly, plasmid was digested with BsmBI-v2 (NEB, R0580) at 55°C for 1 hour.

    Article Title: Targeting leucine-rich repeat kinase 2 overcomes resistance to oncolytic herpes simplex virus-based therapies in glioblastoma.
    Article Snippet: .. The gene encoding human NECTIN1 was synthesized by GENEWIZ and cloned into the LentiCRISPRv2GFP vector, which contains a puromycin selection cassette (Addgene, 82416). .. Constructs expressing human NECTIN1, full-length (FL) LRRK2, truncated LRRK2, FL STAT1, truncated STAT1, and TBK1 were synthesized by GENEWIZ.

    Article Title: Supporting Information for Liver cancer development driven by the AP-1/c-Jun~Fra-2 dimer through c- Myc
    Article Snippet: .. To delete the c-MYC (WRE) enhancer, two flanking CRISPR guides were designed (sg_1: GCCCCTTTGTGGCCTAGGGC and sg_2: GCCCTAGGCCACAAAGGGGC) and cloned into the lentiCRISPR v2 backbone containing a puromycin selection cassette (Addgene#52961) and the resulting plasmid transfected in HepG2 cells using Xtreme gene (Sigma). ..

    Transfection:

    Article Title: Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach.
    Article Snippet: Cells were selected with puromycin (1 ng/μl, Sigma) for 3 days, starting at day 2 after transfection. .. The puromycin selection cassette was subsequently excised by transient transfection of a CRE recombinase expression plasmid pCAG-Cre (Addgene 13,775, [94]). ..

    Article Title: Supporting Information for Liver cancer development driven by the AP-1/c-Jun~Fra-2 dimer through c- Myc
    Article Snippet: .. To delete the c-MYC (WRE) enhancer, two flanking CRISPR guides were designed (sg_1: GCCCCTTTGTGGCCTAGGGC and sg_2: GCCCTAGGCCACAAAGGGGC) and cloned into the lentiCRISPR v2 backbone containing a puromycin selection cassette (Addgene#52961) and the resulting plasmid transfected in HepG2 cells using Xtreme gene (Sigma). ..

    Expressing:

    Article Title: Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach.
    Article Snippet: Cells were selected with puromycin (1 ng/μl, Sigma) for 3 days, starting at day 2 after transfection. .. The puromycin selection cassette was subsequently excised by transient transfection of a CRE recombinase expression plasmid pCAG-Cre (Addgene 13,775, [94]). ..

    Amplification:

    Article Title: The MEMIC is an ex vivo system to model the complexity of the tumor microenvironment
    Article Snippet: To create a hypoxia reporter for live imaging, an existing GFP-based HIF1ɑ reporter (Addgene, 46926 ; ) was subcloned into a lentiviral delivery plasmid using a Gibson assembly-based modular assembly platform (GMAP) ( ). .. The 5xHRE-GFP region and a PGK-driven puromycin selection cassette from the pMSCV-Peredox-mCherry-NLS plasmid (Addgene, 32385 ) were amplified using primers containing overhangs with the homology sites for GMAP cloning and inserted into a lentiviral vector (LV 1-5; Addgene, 68411 ). ..

    Cloning:

    Article Title: The MEMIC is an ex vivo system to model the complexity of the tumor microenvironment
    Article Snippet: To create a hypoxia reporter for live imaging, an existing GFP-based HIF1ɑ reporter (Addgene, 46926 ; ) was subcloned into a lentiviral delivery plasmid using a Gibson assembly-based modular assembly platform (GMAP) ( ). .. The 5xHRE-GFP region and a PGK-driven puromycin selection cassette from the pMSCV-Peredox-mCherry-NLS plasmid (Addgene, 32385 ) were amplified using primers containing overhangs with the homology sites for GMAP cloning and inserted into a lentiviral vector (LV 1-5; Addgene, 68411 ). ..

    Binding Assay:

    Article Title: Complementary constraints in germ and immune cells shape evolution of gene regulation and phenotype
    Article Snippet: .. sgRNAs were designed to target the NGG sites nearest to and flanking the identified CTCF binding domain within the swapped human promoter sequence ( Table S6 ). sgRNAs were cloned into lentiCRISPR v2 plasmid with a Cas9 and puromycin selection cassette (Addgene, 52961; RRID: Addgene_52961) as previously described , . .. Briefly, plasmid was digested with BsmBI-v2 (NEB, R0580) at 55°C for 1 hour.

    Clone Assay:

    Article Title: Complementary constraints in germ and immune cells shape evolution of gene regulation and phenotype
    Article Snippet: .. sgRNAs were designed to target the NGG sites nearest to and flanking the identified CTCF binding domain within the swapped human promoter sequence ( Table S6 ). sgRNAs were cloned into lentiCRISPR v2 plasmid with a Cas9 and puromycin selection cassette (Addgene, 52961; RRID: Addgene_52961) as previously described , . .. Briefly, plasmid was digested with BsmBI-v2 (NEB, R0580) at 55°C for 1 hour.

    Article Title: Targeting leucine-rich repeat kinase 2 overcomes resistance to oncolytic herpes simplex virus-based therapies in glioblastoma.
    Article Snippet: .. The gene encoding human NECTIN1 was synthesized by GENEWIZ and cloned into the LentiCRISPRv2GFP vector, which contains a puromycin selection cassette (Addgene, 82416). .. Constructs expressing human NECTIN1, full-length (FL) LRRK2, truncated LRRK2, FL STAT1, truncated STAT1, and TBK1 were synthesized by GENEWIZ.

    Article Title: Supporting Information for Liver cancer development driven by the AP-1/c-Jun~Fra-2 dimer through c- Myc
    Article Snippet: .. To delete the c-MYC (WRE) enhancer, two flanking CRISPR guides were designed (sg_1: GCCCCTTTGTGGCCTAGGGC and sg_2: GCCCTAGGCCACAAAGGGGC) and cloned into the lentiCRISPR v2 backbone containing a puromycin selection cassette (Addgene#52961) and the resulting plasmid transfected in HepG2 cells using Xtreme gene (Sigma). ..

    Synthesized:

    Article Title: Targeting leucine-rich repeat kinase 2 overcomes resistance to oncolytic herpes simplex virus-based therapies in glioblastoma.
    Article Snippet: .. The gene encoding human NECTIN1 was synthesized by GENEWIZ and cloned into the LentiCRISPRv2GFP vector, which contains a puromycin selection cassette (Addgene, 82416). .. Constructs expressing human NECTIN1, full-length (FL) LRRK2, truncated LRRK2, FL STAT1, truncated STAT1, and TBK1 were synthesized by GENEWIZ.

    CRISPR:

    Article Title: Supporting Information for Liver cancer development driven by the AP-1/c-Jun~Fra-2 dimer through c- Myc
    Article Snippet: .. To delete the c-MYC (WRE) enhancer, two flanking CRISPR guides were designed (sg_1: GCCCCTTTGTGGCCTAGGGC and sg_2: GCCCTAGGCCACAAAGGGGC) and cloned into the lentiCRISPR v2 backbone containing a puromycin selection cassette (Addgene#52961) and the resulting plasmid transfected in HepG2 cells using Xtreme gene (Sigma). ..



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