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recombinant puc 57 plasmids  (Kaneka Corp)

 
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    Kaneka Corp recombinant puc 57 plasmids
    Recombinant Puc 57 Plasmids, supplied by Kaneka Corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+puc+57+plasmids/puc57+plasmid/pm24157887-63-0-4
    Average 90 stars, based on 1 article reviews
    recombinant puc 57 plasmids - by Bioz Stars, 2026-10
    90/100 stars

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    Recombinant:

    Article Title: Real-time PCR systems targeting giant viruses of amoebae and their virophages.
    Article Snippet: .. Recombinant pUC 57 plasmids (Eurogentec, Liège, Belgium) were used as quantification standards, as positive controls and to evaluate the detection limit of the real-time PCR assays. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Real-time PCR systems targeting giant viruses of amoebae and their virophages.
    Article Snippet: .. Recombinant pUC 57 plasmids (Eurogentec, Liège, Belgium) were used as quantification standards, as positive controls and to evaluate the detection limit of the real-time PCR assays. ..



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    recombinant plasmid puc 57 with synthetic dna  (GenScript corporation)
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    GenScript corporation recombinant plasmid puc 57 with synthetic dna
    The pET-26b (+) derived plasmid has a pBR322 origin of replication, which together with the ROP protein regulates the plasmid copy number per bacterial cell. The kanamycin resistance gene enables positive selection of the transformed E . coli cells in the presence of kanamycin. BamHI, EcoRI and HindIII recognition sites, flanking both sites of the T7 promoter, cloning site and T7 terminator cassette, facilitate the screening of the transformed colonies for <t>the</t> <t>recombinant</t> transformants. The cloning site of pET-BccI, composed of two adjacent reverse BccI recognition sites, provides single 5΄-T and C overhangs after digestion with BccI, which are suitable for the ligation of <t>DNA</t> molecules with complementary edges.
    Recombinant Plasmid Puc 57 With Synthetic Dna, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+puc+57+plasmids/puc57/pmc05665511-51-16-18
    Average 90 stars, based on 1 article reviews
    recombinant plasmid puc 57 with synthetic dna - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    recombinant puc 57 plasmids  (Kaneka Corp)
    90
    Kaneka Corp recombinant puc 57 plasmids
    The pET-26b (+) derived plasmid has a pBR322 origin of replication, which together with the ROP protein regulates the plasmid copy number per bacterial cell. The kanamycin resistance gene enables positive selection of the transformed E . coli cells in the presence of kanamycin. BamHI, EcoRI and HindIII recognition sites, flanking both sites of the T7 promoter, cloning site and T7 terminator cassette, facilitate the screening of the transformed colonies for <t>the</t> <t>recombinant</t> transformants. The cloning site of pET-BccI, composed of two adjacent reverse BccI recognition sites, provides single 5΄-T and C overhangs after digestion with BccI, which are suitable for the ligation of <t>DNA</t> molecules with complementary edges.
    Recombinant Puc 57 Plasmids, supplied by Kaneka Corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+puc+57+plasmids/puc57+plasmid/pm24157887-63-0-4
    Average 90 stars, based on 1 article reviews
    recombinant puc 57 plasmids - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

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    The pET-26b (+) derived plasmid has a pBR322 origin of replication, which together with the ROP protein regulates the plasmid copy number per bacterial cell. The kanamycin resistance gene enables positive selection of the transformed E . coli cells in the presence of kanamycin. BamHI, EcoRI and HindIII recognition sites, flanking both sites of the T7 promoter, cloning site and T7 terminator cassette, facilitate the screening of the transformed colonies for the recombinant transformants. The cloning site of pET-BccI, composed of two adjacent reverse BccI recognition sites, provides single 5΄-T and C overhangs after digestion with BccI, which are suitable for the ligation of DNA molecules with complementary edges.

    Journal: PLoS ONE

    Article Title: TA-GC cloning: A new simple and versatile technique for the directional cloning of PCR products for recombinant protein expression

    doi: 10.1371/journal.pone.0186568

    Figure Lengend Snippet: The pET-26b (+) derived plasmid has a pBR322 origin of replication, which together with the ROP protein regulates the plasmid copy number per bacterial cell. The kanamycin resistance gene enables positive selection of the transformed E . coli cells in the presence of kanamycin. BamHI, EcoRI and HindIII recognition sites, flanking both sites of the T7 promoter, cloning site and T7 terminator cassette, facilitate the screening of the transformed colonies for the recombinant transformants. The cloning site of pET-BccI, composed of two adjacent reverse BccI recognition sites, provides single 5΄-T and C overhangs after digestion with BccI, which are suitable for the ligation of DNA molecules with complementary edges.

    Article Snippet: The same digestion reaction was set up using 10 μg of recombinant plasmid pUC 57 with synthetic DNA (Genscript).

    Techniques: Derivative Assay, Plasmid Preparation, Selection, Transformation Assay, Cloning, Recombinant, Ligation