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puromycin selectable marker  (TaKaRa)


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    Structured Review

    TaKaRa puromycin selectable marker
    Puromycin Selectable Marker, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 3509 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/puromycin+selectable+marker/Puromycin/bio_rxiv__2025__06__13__659598-167-25-36
    Average 96 stars, based on 3509 article reviews
    puromycin selectable marker - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Expressing:

    Article Title: Eradication of large established tumors in mice by combination immunotherapy that engages innate and adaptive immune responses
    Article Snippet: Sequences for the sgRNAs ( Supplementary Table 1 ) were designed using tools provided by the Zhang Lab at the Broad Institute (available at http://crispr.mit.edu/ ). .. B16-GFP-Cas9 cells were co-transfected with 2 sgRNAs expression vectors targeting Trp2 and a plasmid expressing EGFP and a puromycin selectable marker from a CAG promoter using Xfect (Clontech) according to manufacturer’s instructions. ..

    Plasmid Preparation:

    Article Title: Eradication of large established tumors in mice by combination immunotherapy that engages innate and adaptive immune responses
    Article Snippet: Sequences for the sgRNAs ( Supplementary Table 1 ) were designed using tools provided by the Zhang Lab at the Broad Institute (available at http://crispr.mit.edu/ ). .. B16-GFP-Cas9 cells were co-transfected with 2 sgRNAs expression vectors targeting Trp2 and a plasmid expressing EGFP and a puromycin selectable marker from a CAG promoter using Xfect (Clontech) according to manufacturer’s instructions. ..

    Article Title: The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes
    Article Snippet: All constructs were confirmed by DNA sequencing. pGEX 6P-4 vector (GE Healthcare Life Science) or pDuet1 His-HRV3C and pDuet1 His-HRV3C-AviTag were used to express GST- or His-tagged proteins, respectively, in bacteria. pEF1a-GST-6P-4 or pEF1a-GST-P-N4 vector was used to express amino terminal or carboxyl terminal GST-tagged proteins in 293T cells. pFLAG-C4 was derived from pMYC-C4 ( ) by replacing the MYC tag with FLAG tag. .. This plasmid was used to transfect 293T for the overexpression of protein. pMSCV-neo MYC-C4 retroviral vector was derived from pMSCV-puro myc vector by replacing the puromycin selectable marker with a neomycin selectable marker from pEGFP-C4 plasmid (Clontech). .. This plasmid was used to make retroviral particles in 293T cells and to express amino terminal MYC tagged protein in mammalian cells. pInducer200 (puro) tet-on EGFP-C4 plasmid was derived from pInducer20 plasmid (Addgene #44012) by: 1) by replacing the tetracycline inducible minimal CMV promoter with the TRE3G promoter from LT3GPIR plasmid (Addgene #111177), 2) inserting EGFP cDNA from pEGFP-C4 (Clontech) plasmid in the downstream of TRE3G promoter, 3) replacing the UbC promoter with the human PGK promoter from pCW-Cas9-Blast plasmid (Addgene #83481), and 4) replacing the neomycin selection marker with the puromycin selection maker cDNA from pMSCV-puro plasmid (Clontech).

    Article Title: Functional Coupling between Secretory and Cytosolic Phospholipase A2 Modulates Tumor Necrosis Factor-α- and Interleukin-1β-induced NF-κB Activation
    Article Snippet: .. HaCaT cells were transfected using the calcium phosphate precipitation procedure according to standard protocols using a 10-fold excess of the plasmid of interest (pBIIX or pfLUC) over the selection plasmid encoding a puromycin selectable marker (pPur; CLONTECH). .. Briefly, each 100-mm plate with HaCaT cells at 50% confluency was co-transfected with 8 g of pBIIX and 0.8 g of pPur (CLONTECH) encoding a puromycin selectable marker.

    Marker:

    Article Title: Eradication of large established tumors in mice by combination immunotherapy that engages innate and adaptive immune responses
    Article Snippet: Sequences for the sgRNAs ( Supplementary Table 1 ) were designed using tools provided by the Zhang Lab at the Broad Institute (available at http://crispr.mit.edu/ ). .. B16-GFP-Cas9 cells were co-transfected with 2 sgRNAs expression vectors targeting Trp2 and a plasmid expressing EGFP and a puromycin selectable marker from a CAG promoter using Xfect (Clontech) according to manufacturer’s instructions. ..

    Article Title: The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes
    Article Snippet: All constructs were confirmed by DNA sequencing. pGEX 6P-4 vector (GE Healthcare Life Science) or pDuet1 His-HRV3C and pDuet1 His-HRV3C-AviTag were used to express GST- or His-tagged proteins, respectively, in bacteria. pEF1a-GST-6P-4 or pEF1a-GST-P-N4 vector was used to express amino terminal or carboxyl terminal GST-tagged proteins in 293T cells. pFLAG-C4 was derived from pMYC-C4 ( ) by replacing the MYC tag with FLAG tag. .. This plasmid was used to transfect 293T for the overexpression of protein. pMSCV-neo MYC-C4 retroviral vector was derived from pMSCV-puro myc vector by replacing the puromycin selectable marker with a neomycin selectable marker from pEGFP-C4 plasmid (Clontech). .. This plasmid was used to make retroviral particles in 293T cells and to express amino terminal MYC tagged protein in mammalian cells. pInducer200 (puro) tet-on EGFP-C4 plasmid was derived from pInducer20 plasmid (Addgene #44012) by: 1) by replacing the tetracycline inducible minimal CMV promoter with the TRE3G promoter from LT3GPIR plasmid (Addgene #111177), 2) inserting EGFP cDNA from pEGFP-C4 (Clontech) plasmid in the downstream of TRE3G promoter, 3) replacing the UbC promoter with the human PGK promoter from pCW-Cas9-Blast plasmid (Addgene #83481), and 4) replacing the neomycin selection marker with the puromycin selection maker cDNA from pMSCV-puro plasmid (Clontech).

    Article Title: Functional Coupling between Secretory and Cytosolic Phospholipase A2 Modulates Tumor Necrosis Factor-α- and Interleukin-1β-induced NF-κB Activation
    Article Snippet: .. HaCaT cells were transfected using the calcium phosphate precipitation procedure according to standard protocols using a 10-fold excess of the plasmid of interest (pBIIX or pfLUC) over the selection plasmid encoding a puromycin selectable marker (pPur; CLONTECH). .. Briefly, each 100-mm plate with HaCaT cells at 50% confluency was co-transfected with 8 g of pBIIX and 0.8 g of pPur (CLONTECH) encoding a puromycin selectable marker.

    Over Expression:

    Article Title: The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes
    Article Snippet: All constructs were confirmed by DNA sequencing. pGEX 6P-4 vector (GE Healthcare Life Science) or pDuet1 His-HRV3C and pDuet1 His-HRV3C-AviTag were used to express GST- or His-tagged proteins, respectively, in bacteria. pEF1a-GST-6P-4 or pEF1a-GST-P-N4 vector was used to express amino terminal or carboxyl terminal GST-tagged proteins in 293T cells. pFLAG-C4 was derived from pMYC-C4 ( ) by replacing the MYC tag with FLAG tag. .. This plasmid was used to transfect 293T for the overexpression of protein. pMSCV-neo MYC-C4 retroviral vector was derived from pMSCV-puro myc vector by replacing the puromycin selectable marker with a neomycin selectable marker from pEGFP-C4 plasmid (Clontech). .. This plasmid was used to make retroviral particles in 293T cells and to express amino terminal MYC tagged protein in mammalian cells. pInducer200 (puro) tet-on EGFP-C4 plasmid was derived from pInducer20 plasmid (Addgene #44012) by: 1) by replacing the tetracycline inducible minimal CMV promoter with the TRE3G promoter from LT3GPIR plasmid (Addgene #111177), 2) inserting EGFP cDNA from pEGFP-C4 (Clontech) plasmid in the downstream of TRE3G promoter, 3) replacing the UbC promoter with the human PGK promoter from pCW-Cas9-Blast plasmid (Addgene #83481), and 4) replacing the neomycin selection marker with the puromycin selection maker cDNA from pMSCV-puro plasmid (Clontech).

    Retroviral:

    Article Title: The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes
    Article Snippet: All constructs were confirmed by DNA sequencing. pGEX 6P-4 vector (GE Healthcare Life Science) or pDuet1 His-HRV3C and pDuet1 His-HRV3C-AviTag were used to express GST- or His-tagged proteins, respectively, in bacteria. pEF1a-GST-6P-4 or pEF1a-GST-P-N4 vector was used to express amino terminal or carboxyl terminal GST-tagged proteins in 293T cells. pFLAG-C4 was derived from pMYC-C4 ( ) by replacing the MYC tag with FLAG tag. .. This plasmid was used to transfect 293T for the overexpression of protein. pMSCV-neo MYC-C4 retroviral vector was derived from pMSCV-puro myc vector by replacing the puromycin selectable marker with a neomycin selectable marker from pEGFP-C4 plasmid (Clontech). .. This plasmid was used to make retroviral particles in 293T cells and to express amino terminal MYC tagged protein in mammalian cells. pInducer200 (puro) tet-on EGFP-C4 plasmid was derived from pInducer20 plasmid (Addgene #44012) by: 1) by replacing the tetracycline inducible minimal CMV promoter with the TRE3G promoter from LT3GPIR plasmid (Addgene #111177), 2) inserting EGFP cDNA from pEGFP-C4 (Clontech) plasmid in the downstream of TRE3G promoter, 3) replacing the UbC promoter with the human PGK promoter from pCW-Cas9-Blast plasmid (Addgene #83481), and 4) replacing the neomycin selection marker with the puromycin selection maker cDNA from pMSCV-puro plasmid (Clontech).

    Derivative Assay:

    Article Title: The nucleus activates mechano-responsiveness via FHOD-associated LINC complexes
    Article Snippet: All constructs were confirmed by DNA sequencing. pGEX 6P-4 vector (GE Healthcare Life Science) or pDuet1 His-HRV3C and pDuet1 His-HRV3C-AviTag were used to express GST- or His-tagged proteins, respectively, in bacteria. pEF1a-GST-6P-4 or pEF1a-GST-P-N4 vector was used to express amino terminal or carboxyl terminal GST-tagged proteins in 293T cells. pFLAG-C4 was derived from pMYC-C4 ( ) by replacing the MYC tag with FLAG tag. .. This plasmid was used to transfect 293T for the overexpression of protein. pMSCV-neo MYC-C4 retroviral vector was derived from pMSCV-puro myc vector by replacing the puromycin selectable marker with a neomycin selectable marker from pEGFP-C4 plasmid (Clontech). .. This plasmid was used to make retroviral particles in 293T cells and to express amino terminal MYC tagged protein in mammalian cells. pInducer200 (puro) tet-on EGFP-C4 plasmid was derived from pInducer20 plasmid (Addgene #44012) by: 1) by replacing the tetracycline inducible minimal CMV promoter with the TRE3G promoter from LT3GPIR plasmid (Addgene #111177), 2) inserting EGFP cDNA from pEGFP-C4 (Clontech) plasmid in the downstream of TRE3G promoter, 3) replacing the UbC promoter with the human PGK promoter from pCW-Cas9-Blast plasmid (Addgene #83481), and 4) replacing the neomycin selection marker with the puromycin selection maker cDNA from pMSCV-puro plasmid (Clontech).

    Transfection:

    Article Title: Functional Coupling between Secretory and Cytosolic Phospholipase A2 Modulates Tumor Necrosis Factor-α- and Interleukin-1β-induced NF-κB Activation
    Article Snippet: .. HaCaT cells were transfected using the calcium phosphate precipitation procedure according to standard protocols using a 10-fold excess of the plasmid of interest (pBIIX or pfLUC) over the selection plasmid encoding a puromycin selectable marker (pPur; CLONTECH). .. Briefly, each 100-mm plate with HaCaT cells at 50% confluency was co-transfected with 8 g of pBIIX and 0.8 g of pPur (CLONTECH) encoding a puromycin selectable marker.

    Selection:

    Article Title: Functional Coupling between Secretory and Cytosolic Phospholipase A2 Modulates Tumor Necrosis Factor-α- and Interleukin-1β-induced NF-κB Activation
    Article Snippet: .. HaCaT cells were transfected using the calcium phosphate precipitation procedure according to standard protocols using a 10-fold excess of the plasmid of interest (pBIIX or pfLUC) over the selection plasmid encoding a puromycin selectable marker (pPur; CLONTECH). .. Briefly, each 100-mm plate with HaCaT cells at 50% confluency was co-transfected with 8 g of pBIIX and 0.8 g of pPur (CLONTECH) encoding a puromycin selectable marker.



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