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in fusion cloning strategy  (TaKaRa)


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    Structured Review

    TaKaRa in fusion cloning strategy
    In Fusion Cloning Strategy, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 1539 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fusion+cloning+strategy/In-Fusion+HD+Cloning+Plus/bio_rxiv__64898__2026__03__30__715387-228-18-21
    Average 99 stars, based on 1539 article reviews
    in fusion cloning strategy - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Construct:

    Article Title: Genetic Analysis of DEFECTIVE KERNEL1 Loop Function in Three-Dimensional Body Patterning in Physcomitrella patens
    Article Snippet: .. To make the corresponding At and Zm Loop complementation constructs, the In-Fusion Cloning Strategy was used (Clontech Laboratory). ..

    Article Title: Campylobacter jejuni Demonstrates Conserved Proteomic and Transcriptomic Responses When Co-cultured With Human INT 407 and Caco-2 Epithelial Cells
    Article Snippet: .. The final constructs were generated using the in-fusion cloning strategy with the In-Fusion HD Cloning Kit (Takara Bio USA Inc. Mountain View, CA, United States), as described previously ( ). ..

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).

    Cloning:

    Article Title: Genetic Analysis of DEFECTIVE KERNEL1 Loop Function in Three-Dimensional Body Patterning in Physcomitrella patens
    Article Snippet: .. To make the corresponding At and Zm Loop complementation constructs, the In-Fusion Cloning Strategy was used (Clontech Laboratory). ..

    Article Title: Campylobacter jejuni Demonstrates Conserved Proteomic and Transcriptomic Responses When Co-cultured With Human INT 407 and Caco-2 Epithelial Cells
    Article Snippet: .. The final constructs were generated using the in-fusion cloning strategy with the In-Fusion HD Cloning Kit (Takara Bio USA Inc. Mountain View, CA, United States), as described previously ( ). ..

    Article Title: 1-Octen-3-ol – the attractant that repels
    Article Snippet: .. The In-Fusion cloning strategy was taken by using In-Fusion ® HD Cloning Kit (Clontech ® Laboratories, Mountain View, CA). ..

    Article Title: Genome-Wide Identification and Analysis of the Valine-Glutamine Motif-Containing Gene Family in Brassica napus and Functional Characterization of BnMKS1 in Response to Leptosphaeria maculans
    Article Snippet: The firststrand cDNA was synthesized from 1 μg total RNA using the first cDNA synthesis Kit (Thermo Scientific, Waltham, MA, USA). .. The in-Fusion cloning strategy was applied to design the overexpression primers to ligate the full-length cDNA of BnMKS1 (BnVQ7: BnaA01g36880D) to pRI201-AN Vector having a CaMV35S promoter (Cat No. 3264, Takara Bio USA) (https://www.takarabio.com/learning-centers/cloning/in-fusion-cloning-tools). ..

    Article Title: Single-stranded HDR templates with truncated Cas12a-binding sequences improve knock-in efficiencies in primary human T cells
    Article Snippet: All plasmid sequences are listed in Table S1; the original CD3ζHDRT and the original TRAC-HDRT are available via Addgene (CD3ζ -truncCARgsg: Addgene ID 215759, TRAC-Cas12a: 215769). www.moleculartherapy.org Molecular Therapy: Nucleic Acids Vol. .. 36 June 2025 11 In-fusion cloning strategy of plasmids The cloning of plasmids encoding HDRTs was conducted using the two-fragment In-Fusion method following the manufacturer’s protocol (Clontech, Takara Bio). ..

    Article Title: Overexpression of <scp><i>BnNAC19</i></scp> in <i>Brassica napus</i> enhances resistance to <i>Leptosphaeria maculans</i>, the blackleg pathogen of canola
    Article Snippet: .. The PCR- amplified BnNAC19 cDNA fragment was ligated to the pRI201- AN overexpression vector harbouring a CaMV 35S promoter using an In- Fusion cloning strategy (Takara Bio Inc.). .. The insertion was confirmed by Sanger sequencing and by digestion with two restriction enzymes, SacI and NdeI (New England Biolabs).

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).

    Generated:

    Article Title: Campylobacter jejuni Demonstrates Conserved Proteomic and Transcriptomic Responses When Co-cultured With Human INT 407 and Caco-2 Epithelial Cells
    Article Snippet: .. The final constructs were generated using the in-fusion cloning strategy with the In-Fusion HD Cloning Kit (Takara Bio USA Inc. Mountain View, CA, United States), as described previously ( ). ..

    Over Expression:

    Article Title: Genome-Wide Identification and Analysis of the Valine-Glutamine Motif-Containing Gene Family in Brassica napus and Functional Characterization of BnMKS1 in Response to Leptosphaeria maculans
    Article Snippet: The firststrand cDNA was synthesized from 1 μg total RNA using the first cDNA synthesis Kit (Thermo Scientific, Waltham, MA, USA). .. The in-Fusion cloning strategy was applied to design the overexpression primers to ligate the full-length cDNA of BnMKS1 (BnVQ7: BnaA01g36880D) to pRI201-AN Vector having a CaMV35S promoter (Cat No. 3264, Takara Bio USA) (https://www.takarabio.com/learning-centers/cloning/in-fusion-cloning-tools). ..

    Article Title: Overexpression of <scp><i>BnNAC19</i></scp> in <i>Brassica napus</i> enhances resistance to <i>Leptosphaeria maculans</i>, the blackleg pathogen of canola
    Article Snippet: .. The PCR- amplified BnNAC19 cDNA fragment was ligated to the pRI201- AN overexpression vector harbouring a CaMV 35S promoter using an In- Fusion cloning strategy (Takara Bio Inc.). .. The insertion was confirmed by Sanger sequencing and by digestion with two restriction enzymes, SacI and NdeI (New England Biolabs).

    Polymerase Chain Reaction:

    Article Title: Overexpression of <scp><i>BnNAC19</i></scp> in <i>Brassica napus</i> enhances resistance to <i>Leptosphaeria maculans</i>, the blackleg pathogen of canola
    Article Snippet: .. The PCR- amplified BnNAC19 cDNA fragment was ligated to the pRI201- AN overexpression vector harbouring a CaMV 35S promoter using an In- Fusion cloning strategy (Takara Bio Inc.). .. The insertion was confirmed by Sanger sequencing and by digestion with two restriction enzymes, SacI and NdeI (New England Biolabs).

    Amplification:

    Article Title: Overexpression of <scp><i>BnNAC19</i></scp> in <i>Brassica napus</i> enhances resistance to <i>Leptosphaeria maculans</i>, the blackleg pathogen of canola
    Article Snippet: .. The PCR- amplified BnNAC19 cDNA fragment was ligated to the pRI201- AN overexpression vector harbouring a CaMV 35S promoter using an In- Fusion cloning strategy (Takara Bio Inc.). .. The insertion was confirmed by Sanger sequencing and by digestion with two restriction enzymes, SacI and NdeI (New England Biolabs).

    Plasmid Preparation:

    Article Title: Overexpression of <scp><i>BnNAC19</i></scp> in <i>Brassica napus</i> enhances resistance to <i>Leptosphaeria maculans</i>, the blackleg pathogen of canola
    Article Snippet: .. The PCR- amplified BnNAC19 cDNA fragment was ligated to the pRI201- AN overexpression vector harbouring a CaMV 35S promoter using an In- Fusion cloning strategy (Takara Bio Inc.). .. The insertion was confirmed by Sanger sequencing and by digestion with two restriction enzymes, SacI and NdeI (New England Biolabs).

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).

    FLAG-tag:

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).

    Clone Assay:

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).

    Expressing:

    Article Title: CD147: a small molecule transporter ancillary protein at the crossroad of multiple hallmarks of cancer and metabolic reprogramming
    Article Snippet: Point mutations and deletion constructs were generated with Quick Change Site directed mutagenesis kit (Agilent Technologies, Santa Clara, CA) according to manufacturer's description. .. For CD147-ECD construct residues corresponding to a signal peptide (amino acids 1-21 of human CD147) followed by FLAG tag, 6xHis affinity tag, a TEV cleavage site, and amino acids 22-2-5 of human CD147, were cloned into a mammalian expression vector (pCEP4, Invitrogen) between NdeI and BamH1 sites using In Fusion cloning strategy (Clontech). pMM2-hPMCA1b was a gift from John Penniston & Emanuel Strehler (Addgene plasmid #47758). .. To generate pMM2-hPMCA1b-GFP plasmid, GFP was PCR amplified from pcDNA3.1-GFP plasmid and inserted using KpnI site (In-Fusion Cloning, Clontech).



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