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plasmid hsp83 promoter fragment mini- yellow coding sequence p10 terminator  (Addgene inc)


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    Structured Review

    Addgene inc plasmid hsp83 promoter fragment mini- yellow coding sequence p10 terminator
    Plasmid Hsp83 Promoter Fragment Mini Yellow Coding Sequence P10 Terminator, supplied by Addgene inc, 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/promoter+fragment+sequence/plasmid+hsp83+promoter+fragment+mini++yellow+coding+sequence+p10+terminator/bio_rxiv__2025__03__30__646185-233-7-34
    Average 90 stars, based on 1 article reviews
    plasmid hsp83 promoter fragment mini- yellow coding sequence p10 terminator - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Engineered reproductively isolated species drive reversible population replacement.
    Article Snippet: .. First, the plasmid was digested with AsiSI and KpnI, and the following components were cloned in with EA cloning to generate base plasmid OA-1045: a D. melanogaster U6:3 promoter fragment sequence amplified from Addgene plasmid #4941126 with primers 1045.C1 and 1045.C2, and an sgRNA scaffold fragment amplified from Addgene plasmid #4941126 with primers 1045.C3 and 1045.C4. ..

    Clone Assay:

    Article Title: Engineered reproductively isolated species drive reversible population replacement.
    Article Snippet: .. First, the plasmid was digested with AsiSI and KpnI, and the following components were cloned in with EA cloning to generate base plasmid OA-1045: a D. melanogaster U6:3 promoter fragment sequence amplified from Addgene plasmid #4941126 with primers 1045.C1 and 1045.C2, and an sgRNA scaffold fragment amplified from Addgene plasmid #4941126 with primers 1045.C3 and 1045.C4. ..

    Cloning:

    Article Title: Engineered reproductively isolated species drive reversible population replacement.
    Article Snippet: .. First, the plasmid was digested with AsiSI and KpnI, and the following components were cloned in with EA cloning to generate base plasmid OA-1045: a D. melanogaster U6:3 promoter fragment sequence amplified from Addgene plasmid #4941126 with primers 1045.C1 and 1045.C2, and an sgRNA scaffold fragment amplified from Addgene plasmid #4941126 with primers 1045.C3 and 1045.C4. ..

    Sequencing:

    Article Title: Engineered reproductively isolated species drive reversible population replacement.
    Article Snippet: .. First, the plasmid was digested with AsiSI and KpnI, and the following components were cloned in with EA cloning to generate base plasmid OA-1045: a D. melanogaster U6:3 promoter fragment sequence amplified from Addgene plasmid #4941126 with primers 1045.C1 and 1045.C2, and an sgRNA scaffold fragment amplified from Addgene plasmid #4941126 with primers 1045.C3 and 1045.C4. ..

    Amplification:

    Article Title: Engineered reproductively isolated species drive reversible population replacement.
    Article Snippet: .. First, the plasmid was digested with AsiSI and KpnI, and the following components were cloned in with EA cloning to generate base plasmid OA-1045: a D. melanogaster U6:3 promoter fragment sequence amplified from Addgene plasmid #4941126 with primers 1045.C1 and 1045.C2, and an sgRNA scaffold fragment amplified from Addgene plasmid #4941126 with primers 1045.C3 and 1045.C4. ..



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