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recombinant plasmids pet28a-tat-hsp27  (Enzynomics co Ltd)

 
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    Enzynomics co Ltd recombinant plasmids pet28a-tat-hsp27
    Recombinant Plasmids Pet28a Tat Hsp27, supplied by Enzynomics co Ltd, 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/pet+28a+++expression+vector/pet+28a++++vector/pmc04572059-31-2-17
    Average 90 stars, based on 1 article reviews
    recombinant plasmids pet28a-tat-hsp27 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Recombinant:

    Article Title:
    Article Snippet: .. The recombinant plasmids (pET28a-Tat-Hsp27, pET28a-Hsp27) were transformed into the Escherichia coli strain BL21 (DE3) for protein expression (Enzynomics, Korea). ..

    Transformation Assay:

    Article Title:
    Article Snippet: .. The recombinant plasmids (pET28a-Tat-Hsp27, pET28a-Hsp27) were transformed into the Escherichia coli strain BL21 (DE3) for protein expression (Enzynomics, Korea). ..

    Expressing:

    Article Title:
    Article Snippet: .. The recombinant plasmids (pET28a-Tat-Hsp27, pET28a-Hsp27) were transformed into the Escherichia coli strain BL21 (DE3) for protein expression (Enzynomics, Korea). ..



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    Image Search Results


    (A) In silico cloning of the vaccine construct sequence into the pET-28a (+) expression vector. The construct sequence (blue) was cloned between the vector's EcoRI and BamHI restriction sites (black). (B) 1% agarose gel electrophoresis simulation. The lanes show the molecular weight (MW), and the cloning results in positions 1–3, where lane 1, lane 2, and lane 3 represent the vaccine construct (888bp), the pET-28a (+) (5369bp), and the recombinant plasmid (6245bp), respectively.

    Journal: Journal of Immunology Research

    Article Title: In Silico Design and Characterization of a Multiepitope Vaccine Candidate Against Brucella canis Using a Reverse Vaccinology Approach

    doi: 10.1155/jimr/6348238

    Figure Lengend Snippet: (A) In silico cloning of the vaccine construct sequence into the pET-28a (+) expression vector. The construct sequence (blue) was cloned between the vector's EcoRI and BamHI restriction sites (black). (B) 1% agarose gel electrophoresis simulation. The lanes show the molecular weight (MW), and the cloning results in positions 1–3, where lane 1, lane 2, and lane 3 represent the vaccine construct (888bp), the pET-28a (+) (5369bp), and the recombinant plasmid (6245bp), respectively.

    Article Snippet: The pET-28a (+) expression vector, obtained from the Addgene database ( https://www.addgene.org/ ) [ ], was selected as the cloning vector.

    Techniques: In Silico, Cloning, Construct, Sequencing, Expressing, Plasmid Preparation, Clone Assay, Agarose Gel Electrophoresis, Molecular Weight, Recombinant