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gibson assembly master mix  (New England Biolabs)


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    Structured Review

    New England Biolabs gibson assembly master mix
    Gibson Assembly Master Mix, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 6210 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gibson+assembly+master+mix/Gibson+Assembly+Master+Mix/pmc12967149-217-24-28
    Average 99 stars, based on 6210 article reviews
    gibson assembly master mix - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Polymerase Chain Reaction:

    Article Title: AI platform for CRISPR functional mapping and function-based drug design
    Article Snippet: The sgRNA oligos were amplified with PCR using Phusion High-Fidelity DNA Polymerase (NEB, M0530S). .. The PCR product was then gel purified using QIAquick Gel Extraction Kit (QIAGEN, 28704) and cloned using 10ng of PCR product and 25ng of digested pHKO9 for a 20μl reaction using a Gibson Assembly Master Mix (NEB, E2611S) leaving it at 50C for 60 minutes and 12C after. .. 1μl of the Gibson Assembly reaction was then added to 25 μl of E.Cloni (Biosearch Technologies, 60107-1) for electroporation using a 1mm Cuvette (Bio-Rad, 165-2089) at 25μF, 200 Ohms, and 1500 volts.

    Article Title: Development of a tetracycline-inducible programmed ribosomal frameshifting platform for sensitive regulation of mammalian gene expression
    Article Snippet: .. The constructs were created using overhang extension polymerase chain reaction (PCR), followed by ligation with the Quick LigationTM Kit (NEB) or the Gibson assembly of PCR-amplified vector backbones and inserts in 2× Gibson Assembly Master Mix (NEB). .. All oligonucleotides were ordered from Sigma–Aldrich.

    Purification:

    Article Title: AI platform for CRISPR functional mapping and function-based drug design
    Article Snippet: The sgRNA oligos were amplified with PCR using Phusion High-Fidelity DNA Polymerase (NEB, M0530S). .. The PCR product was then gel purified using QIAquick Gel Extraction Kit (QIAGEN, 28704) and cloned using 10ng of PCR product and 25ng of digested pHKO9 for a 20μl reaction using a Gibson Assembly Master Mix (NEB, E2611S) leaving it at 50C for 60 minutes and 12C after. .. 1μl of the Gibson Assembly reaction was then added to 25 μl of E.Cloni (Biosearch Technologies, 60107-1) for electroporation using a 1mm Cuvette (Bio-Rad, 165-2089) at 25μF, 200 Ohms, and 1500 volts.

    Article Title: Development of a suite of activatable plant synthetic promoter systems using a bacterial LysR-type transcriptional regulator FdeR
    Article Snippet: .. Briefly, DNA fragments were amplified from template plasmids or synthesized DNA fragments (listed in ) via the Q5 polymerase (New England BioLabs), purified with the Zymoclean gel DNA recovery kit (Zymo Research), and assembled with the Gibson Assembly Master Mix (New England BioLabs), according to the manufacturer's instructions. ..

    Gel Extraction:

    Article Title: AI platform for CRISPR functional mapping and function-based drug design
    Article Snippet: The sgRNA oligos were amplified with PCR using Phusion High-Fidelity DNA Polymerase (NEB, M0530S). .. The PCR product was then gel purified using QIAquick Gel Extraction Kit (QIAGEN, 28704) and cloned using 10ng of PCR product and 25ng of digested pHKO9 for a 20μl reaction using a Gibson Assembly Master Mix (NEB, E2611S) leaving it at 50C for 60 minutes and 12C after. .. 1μl of the Gibson Assembly reaction was then added to 25 μl of E.Cloni (Biosearch Technologies, 60107-1) for electroporation using a 1mm Cuvette (Bio-Rad, 165-2089) at 25μF, 200 Ohms, and 1500 volts.

    Clone Assay:

    Article Title: AI platform for CRISPR functional mapping and function-based drug design
    Article Snippet: The sgRNA oligos were amplified with PCR using Phusion High-Fidelity DNA Polymerase (NEB, M0530S). .. The PCR product was then gel purified using QIAquick Gel Extraction Kit (QIAGEN, 28704) and cloned using 10ng of PCR product and 25ng of digested pHKO9 for a 20μl reaction using a Gibson Assembly Master Mix (NEB, E2611S) leaving it at 50C for 60 minutes and 12C after. .. 1μl of the Gibson Assembly reaction was then added to 25 μl of E.Cloni (Biosearch Technologies, 60107-1) for electroporation using a 1mm Cuvette (Bio-Rad, 165-2089) at 25μF, 200 Ohms, and 1500 volts.

    Transformation Assay:

    Article Title: Zebrafish Ace2N-mNeon expression toolkit for in vivo voltage imaging of neuronal synchrony and cardiac maturation
    Article Snippet: Inserts were generated by overlap-extension PCR using Phusion high-fidelity DNA polymerase (NEB), and promoter-containing backbones were amplified with KOD Xtreme Hot Start DNA Polymerase (Merck Sigma). .. Fragments were assembled with Gibson Assembly Master Mix (NEB) and transformed into NEB ® 5-alpha competent E. coli . ..

    Plasmid Preparation:

    Article Title: The nuclear envelope protein TMEM209 is an integral component of the nuclear pore complex and interacts with Nup210
    Article Snippet: .. For the Gibson assembly method, 50 ng of vector DNA was mixed with a 3-fold molar excess of insert DNA and 10 μl 2× Gibson Assembly Master Mix (New England Biolabs) in a total volume of 20 μl. ..

    Article Title: Development of a tetracycline-inducible programmed ribosomal frameshifting platform for sensitive regulation of mammalian gene expression
    Article Snippet: .. The constructs were created using overhang extension polymerase chain reaction (PCR), followed by ligation with the Quick LigationTM Kit (NEB) or the Gibson assembly of PCR-amplified vector backbones and inserts in 2× Gibson Assembly Master Mix (NEB). .. All oligonucleotides were ordered from Sigma–Aldrich.

    Construct:

    Article Title: Differential tolerance for SEA domain misfolding encodes a MAPK pathway-specific response
    Article Snippet: .. Plasmids were constructed by gap repair and Gibson Assembly [( G ibson et al . 2009 ), Gibson Assembly Master Mix, New England Biolabs, Beverly MA, Catalog # E5510S]. ..

    Article Title: Development of a tetracycline-inducible programmed ribosomal frameshifting platform for sensitive regulation of mammalian gene expression
    Article Snippet: .. The constructs were created using overhang extension polymerase chain reaction (PCR), followed by ligation with the Quick LigationTM Kit (NEB) or the Gibson assembly of PCR-amplified vector backbones and inserts in 2× Gibson Assembly Master Mix (NEB). .. All oligonucleotides were ordered from Sigma–Aldrich.

    Amplification:

    Article Title: Development of a suite of activatable plant synthetic promoter systems using a bacterial LysR-type transcriptional regulator FdeR
    Article Snippet: .. Briefly, DNA fragments were amplified from template plasmids or synthesized DNA fragments (listed in ) via the Q5 polymerase (New England BioLabs), purified with the Zymoclean gel DNA recovery kit (Zymo Research), and assembled with the Gibson Assembly Master Mix (New England BioLabs), according to the manufacturer's instructions. ..

    Synthesized:

    Article Title: Development of a suite of activatable plant synthetic promoter systems using a bacterial LysR-type transcriptional regulator FdeR
    Article Snippet: .. Briefly, DNA fragments were amplified from template plasmids or synthesized DNA fragments (listed in ) via the Q5 polymerase (New England BioLabs), purified with the Zymoclean gel DNA recovery kit (Zymo Research), and assembled with the Gibson Assembly Master Mix (New England BioLabs), according to the manufacturer's instructions. ..

    Ligation:

    Article Title: Development of a tetracycline-inducible programmed ribosomal frameshifting platform for sensitive regulation of mammalian gene expression
    Article Snippet: .. The constructs were created using overhang extension polymerase chain reaction (PCR), followed by ligation with the Quick LigationTM Kit (NEB) or the Gibson assembly of PCR-amplified vector backbones and inserts in 2× Gibson Assembly Master Mix (NEB). .. All oligonucleotides were ordered from Sigma–Aldrich.



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