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t5 promoter lac operator element  (Genovis Inc)


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Bioz Manufacturer Symbol Genovis Inc manufactures this product  
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    Structured Review

    Genovis Inc t5 promoter lac operator element
    T5 Promoter Lac Operator Element, supplied by Genovis Inc, used in various techniques. Bioz Stars score: 93/100, based on 92 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/t5+promoter+lac+operator+element/OpeRATOR+Lyophilized/pm19035630__ja806668q_si_001-8-54-56
    Average 93 stars, based on 92 article reviews
    t5 promoter lac operator element - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Produced:

    Article Title:
    Article Snippet: .. A synthetic gene encoding the LytB protein of A. aeolicus in the preferred codon usage of E. coli was produced by custom synthesis (Eurofins Medigenomix): ccATGGTGGATATCATTATTGCCGAACATGCCGGTTTCTGTTTCGGTGTCAAAC GTGCAGTTAAGCTGGCGGAAGAGTCCCTGAAAGAGAGCCAAGGCAAAGTCT ATACCCTGGGCCCGATCATTCATAATCCGCAAGAAGTGAACCGCCTGAAAAA CCTGGGCGTGTTTCCATCTCAGGGTGAAGAATTTAAAGAAGGCGATACCGTC ATTATCCGCTCACATGGCATTCCGCCGGAAAAAGAAGAAGCGCTGCGCAAAA AAGGCCTGAAGGTGATTGACGCGACGTGCCCTTACGTGAAAGCGGTTCACGA AGCGGTGTGTCAACTGACGCGTGAAGGTTACTTTGTGGTCCTGGTCGGCGAG AAAAATCACCCGGAAGTGATCGGTACGCTGGGCTATCTGCGCGCGTGCAACG GCAAGGGTATTGTCGTTGAAACTCTGGAGGATATCGGTGAGGCACTGAAACA TGAACGTGTGGGTATCGTTGCGCAAACGACCCAGAATGAAGAATTTTTTAAG GAAGTGGTGGGTGAAATTGCCCTGTGGGTGAAAGAGGTTAAAGTTATCAATA CCATCTGTAACGCAACCTCGCTGCGCCAGGAATCTGTTAAAAAACTGGCCCC AGAGGTTGACGTCATGATTATTATTGGTGGCAAGAACAGTGGCAACACCCGC CGTCTGTATTACATCTCAAAAGAACTGAATCCGAATACTTATCACATTGAAAC TGCCGAGGAGCTtCAGCCGGAATGGTTCCGCGGCGTGAAGCGTGTTGGCATTT CGGCAGGTGCGTCCACCCCTGATTGGATCATCGAACAGGTCAAAAGCCGTAT CCAGGAAATCTGCGAGGGTCAGCTGGTCAGCAGTagatct The synthetic gene was cloned into the pQE60 vector (Qiagen) issuing a T5 promoter/lac operator element, using Nco I and Bgl II restriction sites. .. After this construct proved to be unstable in E. coli cells (presumably due to leaky expression), the gene was re-cloned into the tetracycline inducible pASK-IBA33-plus vector (IBA, Göttingen, Germany).

    Clone Assay:

    Article Title:
    Article Snippet: .. A synthetic gene encoding the LytB protein of A. aeolicus in the preferred codon usage of E. coli was produced by custom synthesis (Eurofins Medigenomix): ccATGGTGGATATCATTATTGCCGAACATGCCGGTTTCTGTTTCGGTGTCAAAC GTGCAGTTAAGCTGGCGGAAGAGTCCCTGAAAGAGAGCCAAGGCAAAGTCT ATACCCTGGGCCCGATCATTCATAATCCGCAAGAAGTGAACCGCCTGAAAAA CCTGGGCGTGTTTCCATCTCAGGGTGAAGAATTTAAAGAAGGCGATACCGTC ATTATCCGCTCACATGGCATTCCGCCGGAAAAAGAAGAAGCGCTGCGCAAAA AAGGCCTGAAGGTGATTGACGCGACGTGCCCTTACGTGAAAGCGGTTCACGA AGCGGTGTGTCAACTGACGCGTGAAGGTTACTTTGTGGTCCTGGTCGGCGAG AAAAATCACCCGGAAGTGATCGGTACGCTGGGCTATCTGCGCGCGTGCAACG GCAAGGGTATTGTCGTTGAAACTCTGGAGGATATCGGTGAGGCACTGAAACA TGAACGTGTGGGTATCGTTGCGCAAACGACCCAGAATGAAGAATTTTTTAAG GAAGTGGTGGGTGAAATTGCCCTGTGGGTGAAAGAGGTTAAAGTTATCAATA CCATCTGTAACGCAACCTCGCTGCGCCAGGAATCTGTTAAAAAACTGGCCCC AGAGGTTGACGTCATGATTATTATTGGTGGCAAGAACAGTGGCAACACCCGC CGTCTGTATTACATCTCAAAAGAACTGAATCCGAATACTTATCACATTGAAAC TGCCGAGGAGCTtCAGCCGGAATGGTTCCGCGGCGTGAAGCGTGTTGGCATTT CGGCAGGTGCGTCCACCCCTGATTGGATCATCGAACAGGTCAAAAGCCGTAT CCAGGAAATCTGCGAGGGTCAGCTGGTCAGCAGTagatct The synthetic gene was cloned into the pQE60 vector (Qiagen) issuing a T5 promoter/lac operator element, using Nco I and Bgl II restriction sites. .. After this construct proved to be unstable in E. coli cells (presumably due to leaky expression), the gene was re-cloned into the tetracycline inducible pASK-IBA33-plus vector (IBA, Göttingen, Germany).

    Plasmid Preparation:

    Article Title:
    Article Snippet: .. A synthetic gene encoding the LytB protein of A. aeolicus in the preferred codon usage of E. coli was produced by custom synthesis (Eurofins Medigenomix): ccATGGTGGATATCATTATTGCCGAACATGCCGGTTTCTGTTTCGGTGTCAAAC GTGCAGTTAAGCTGGCGGAAGAGTCCCTGAAAGAGAGCCAAGGCAAAGTCT ATACCCTGGGCCCGATCATTCATAATCCGCAAGAAGTGAACCGCCTGAAAAA CCTGGGCGTGTTTCCATCTCAGGGTGAAGAATTTAAAGAAGGCGATACCGTC ATTATCCGCTCACATGGCATTCCGCCGGAAAAAGAAGAAGCGCTGCGCAAAA AAGGCCTGAAGGTGATTGACGCGACGTGCCCTTACGTGAAAGCGGTTCACGA AGCGGTGTGTCAACTGACGCGTGAAGGTTACTTTGTGGTCCTGGTCGGCGAG AAAAATCACCCGGAAGTGATCGGTACGCTGGGCTATCTGCGCGCGTGCAACG GCAAGGGTATTGTCGTTGAAACTCTGGAGGATATCGGTGAGGCACTGAAACA TGAACGTGTGGGTATCGTTGCGCAAACGACCCAGAATGAAGAATTTTTTAAG GAAGTGGTGGGTGAAATTGCCCTGTGGGTGAAAGAGGTTAAAGTTATCAATA CCATCTGTAACGCAACCTCGCTGCGCCAGGAATCTGTTAAAAAACTGGCCCC AGAGGTTGACGTCATGATTATTATTGGTGGCAAGAACAGTGGCAACACCCGC CGTCTGTATTACATCTCAAAAGAACTGAATCCGAATACTTATCACATTGAAAC TGCCGAGGAGCTtCAGCCGGAATGGTTCCGCGGCGTGAAGCGTGTTGGCATTT CGGCAGGTGCGTCCACCCCTGATTGGATCATCGAACAGGTCAAAAGCCGTAT CCAGGAAATCTGCGAGGGTCAGCTGGTCAGCAGTagatct The synthetic gene was cloned into the pQE60 vector (Qiagen) issuing a T5 promoter/lac operator element, using Nco I and Bgl II restriction sites. .. After this construct proved to be unstable in E. coli cells (presumably due to leaky expression), the gene was re-cloned into the tetracycline inducible pASK-IBA33-plus vector (IBA, Göttingen, Germany).



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