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gibson assembly cloning kit  (New England Biolabs)


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    New England Biolabs gibson assembly cloning kit
    Gibson Assembly Cloning Kit, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 4143 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gibson+assembly+cloning+kit/Gibson+Assembly+Cloning+Kit/pmc13652249-465-15-19
    Average 99 stars, based on 4143 article reviews
    gibson assembly cloning kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Temporal loss of En1 during limb development causes distinct phenotypes
    Article Snippet: .. The SYN72 vector (pCMV-SynA [Addgene plasmid 174860]) was linearized by digestion with PacI (NEB), and the LSEE1&2 insert was integrated using the Gibson Assembly cloning kit (NEB). ..

    Article Title: Engineering an Optogenetic pH-Modulator in Bacteria.
    Article Snippet: .. Genes were inserted into the pAB50 plasmid backbone (Addgene) using PCR amplification followed by NEB Gibson Assembly cloning kit. pOpto-T7 Urease variants were then transformed into One Shot Mach T1 chemically competent E. coli cells following the provider’s protocol. .. Constructs were isolated using the QIAprep Spin Miniprep Kit and sequenced using nanopore sequencing (Twist Biosciences). pOpto-T7 Urease degradation tag variants were synthesized using Twist Biosciences, followed by the cloning steps stated above.

    Cloning:

    Article Title: Temporal loss of En1 during limb development causes distinct phenotypes
    Article Snippet: .. The SYN72 vector (pCMV-SynA [Addgene plasmid 174860]) was linearized by digestion with PacI (NEB), and the LSEE1&2 insert was integrated using the Gibson Assembly cloning kit (NEB). ..

    Article Title: Engineering an Optogenetic pH-Modulator in Bacteria.
    Article Snippet: .. Genes were inserted into the pAB50 plasmid backbone (Addgene) using PCR amplification followed by NEB Gibson Assembly cloning kit. pOpto-T7 Urease variants were then transformed into One Shot Mach T1 chemically competent E. coli cells following the provider’s protocol. .. Constructs were isolated using the QIAprep Spin Miniprep Kit and sequenced using nanopore sequencing (Twist Biosciences). pOpto-T7 Urease degradation tag variants were synthesized using Twist Biosciences, followed by the cloning steps stated above.

    Article Title: In Situ Genetic Engineering Facilitates MMP-9-Responsive TIMP1 Release Through Proteolytic Cleavage to Boost Diabetic Wound Healing.
    Article Snippet: .. Plasmids used in this study were constructed via Gibson assembly using the Gibson Assembly Cloning Kit (New England BioLabs, MA, USA). ..

    Article Title: New insights into Müllerian duct differentiation provided by single cell transcriptomics in the chicken embryo
    Article Snippet: .. To generate the AMH overexpression construct, emGFP-T2A-cAMH was cloned into the RCASBP(A) vector using the Gibson Assembly Cloning kit (New England Biolabs), as previously described [ ]. .. This is a method for inducing ubiquitous gene expression using the avian retroviral vector, Replication-Competent Avian sarcoma-leukosis virus, with a Splice acceptor, Bryan RSV Pol (RCASBP).

    Article Title: Programmable histone acetylation enables reversible regulation of cellulase production in Myceliophthora thermophila.
    Article Snippet: PCR amplification was performed using Super-Fidelity DNA Polymerase (Vazyme, Nanjing, China). .. Plasmids were assembled using the Gibson Assembly Cloning Kit (New England Biolabs, Beijing, China). .. A codon-optimized dCas9 gene, XTEN80 linker and p300 core gene were synthesized by Life Sciences Research Services (Genewiz, Suzhou, China).

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    Polymerase Chain Reaction:

    Article Title: ARHGAP18 complexes with both YAP and Merlin and is required for basal actin bundles.
    Article Snippet: The organization of the cell’s cytoskeletal filaments is coordinated through a complex network of signaling cascades activated by both internal and external cues.. Two major actin regulatory pathways are signal transduction through Rho family GTPases and growth and proliferation signaling through the Hippo pathway.. These two pathways define the actin cytoskeleton, controlling foundational cellular attributes such as morphology, the organization of actin-based structures, and are hijacked to promote proliferation and motility in aggressive cancers.

    Article Title: Engineering an Optogenetic pH-Modulator in Bacteria.
    Article Snippet: .. Genes were inserted into the pAB50 plasmid backbone (Addgene) using PCR amplification followed by NEB Gibson Assembly cloning kit. pOpto-T7 Urease variants were then transformed into One Shot Mach T1 chemically competent E. coli cells following the provider’s protocol. .. Constructs were isolated using the QIAprep Spin Miniprep Kit and sequenced using nanopore sequencing (Twist Biosciences). pOpto-T7 Urease degradation tag variants were synthesized using Twist Biosciences, followed by the cloning steps stated above.

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    Gel Extraction:

    Article Title: ARHGAP18 complexes with both YAP and Merlin and is required for basal actin bundles.
    Article Snippet: The organization of the cell’s cytoskeletal filaments is coordinated through a complex network of signaling cascades activated by both internal and external cues.. Two major actin regulatory pathways are signal transduction through Rho family GTPases and growth and proliferation signaling through the Hippo pathway.. These two pathways define the actin cytoskeleton, controlling foundational cellular attributes such as morphology, the organization of actin-based structures, and are hijacked to promote proliferation and motility in aggressive cancers.

    Amplification:

    Article Title: Engineering an Optogenetic pH-Modulator in Bacteria.
    Article Snippet: .. Genes were inserted into the pAB50 plasmid backbone (Addgene) using PCR amplification followed by NEB Gibson Assembly cloning kit. pOpto-T7 Urease variants were then transformed into One Shot Mach T1 chemically competent E. coli cells following the provider’s protocol. .. Constructs were isolated using the QIAprep Spin Miniprep Kit and sequenced using nanopore sequencing (Twist Biosciences). pOpto-T7 Urease degradation tag variants were synthesized using Twist Biosciences, followed by the cloning steps stated above.

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    Transformation Assay:

    Article Title: Engineering an Optogenetic pH-Modulator in Bacteria.
    Article Snippet: .. Genes were inserted into the pAB50 plasmid backbone (Addgene) using PCR amplification followed by NEB Gibson Assembly cloning kit. pOpto-T7 Urease variants were then transformed into One Shot Mach T1 chemically competent E. coli cells following the provider’s protocol. .. Constructs were isolated using the QIAprep Spin Miniprep Kit and sequenced using nanopore sequencing (Twist Biosciences). pOpto-T7 Urease degradation tag variants were synthesized using Twist Biosciences, followed by the cloning steps stated above.

    Construct:

    Article Title: In Situ Genetic Engineering Facilitates MMP-9-Responsive TIMP1 Release Through Proteolytic Cleavage to Boost Diabetic Wound Healing.
    Article Snippet: .. Plasmids used in this study were constructed via Gibson assembly using the Gibson Assembly Cloning Kit (New England BioLabs, MA, USA). ..

    Article Title: New insights into Müllerian duct differentiation provided by single cell transcriptomics in the chicken embryo
    Article Snippet: .. To generate the AMH overexpression construct, emGFP-T2A-cAMH was cloned into the RCASBP(A) vector using the Gibson Assembly Cloning kit (New England Biolabs), as previously described [ ]. .. This is a method for inducing ubiquitous gene expression using the avian retroviral vector, Replication-Competent Avian sarcoma-leukosis virus, with a Splice acceptor, Bryan RSV Pol (RCASBP).

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    Over Expression:

    Article Title: New insights into Müllerian duct differentiation provided by single cell transcriptomics in the chicken embryo
    Article Snippet: .. To generate the AMH overexpression construct, emGFP-T2A-cAMH was cloned into the RCASBP(A) vector using the Gibson Assembly Cloning kit (New England Biolabs), as previously described [ ]. .. This is a method for inducing ubiquitous gene expression using the avian retroviral vector, Replication-Competent Avian sarcoma-leukosis virus, with a Splice acceptor, Bryan RSV Pol (RCASBP).

    Clone Assay:

    Article Title: New insights into Müllerian duct differentiation provided by single cell transcriptomics in the chicken embryo
    Article Snippet: .. To generate the AMH overexpression construct, emGFP-T2A-cAMH was cloned into the RCASBP(A) vector using the Gibson Assembly Cloning kit (New England Biolabs), as previously described [ ]. .. This is a method for inducing ubiquitous gene expression using the avian retroviral vector, Replication-Competent Avian sarcoma-leukosis virus, with a Splice acceptor, Bryan RSV Pol (RCASBP).

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    other:

    Article Title: Triptans reprogram Schwann cells to drive medication-overuse headache via β-glycan/TGF-β3 signaling
    Article Snippet: From pCAG-G-FLAMP2 (#192782, RRID:Addgene_192782, Addgene), G-FLAMP2 was cloned (EcoRI/XbaI) into pEG backbone (P33/P34).

    Stable Transfection:

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..

    Expressing:

    Article Title: Somatic mutations in CSK disrupt immune regulation in a Chinese aplastic anemia cohort.
    Article Snippet: .. To construct cells stably over-expressing CSK, full-length wild-type CSK cDNA was amplified from one patient DNA by PCR and cloned into a lentiviral expression vector (pLenti-CMV-GFP-Puro; Addgene, #17448) using the Gibson Assembly Cloning Kit (New England Biolabs, E5510), according to the manufacturer’s instructions. ..



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