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hind iii  (TaKaRa)


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    Structured Review

    TaKaRa hind iii
    Hind Iii, supplied by TaKaRa, used in various techniques. Bioz Stars score: 99/100, based on 9130 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hind+iii/Hind+III/us12630855-245-16-18
    Average 99 stars, based on 9130 article reviews
    hind iii - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Expressing:

    Article Title: Effects of TRIB3 gene overexpression and interference on lipid metabolism in mammary epithelial cells of yaks
    Article Snippet: The empty plasmid was extracted from the bacterial solution of pcDNA3.1 (+) plasmid (V79020, Invitrogen) stored in the laboratory using the High purity plasmid medium kit (EM101-01, full Gold) after amplification. .. The eukaryotic expression vector pcDNA3.1 (+) and purified PCR products were then digested with Hind III (1060S, TAKARA) and Xba I (1093S, TAKARA) restriction enzymes for 2 h at 37 °C. ..

    Article Title: PRSS23 Promotes Ovarian Follicular Atresia in Wuding Chickens by Coordinately Suppressing Steroidogenesis and PI3K/AKT/mTOR Survival Signaling
    Article Snippet: For overexpression studies, the CDS of PRSS23 was amplified from Wuding chicken ovarian cDNA using gene-specific primers ( ) and subsequently cloned into the pMD-18T vector (TaKaRa). .. The insert was then excised by double digestion with Kpn I and Hind III, gel-purified, and ligated into the EGFP expression vector (Clontech Laboratories, Palo Alto, CA, USA). ..

    Article Title: PRSS23 Promotes Ovarian Follicular Atresia in Wuding Chickens by Coordinately Suppressing Steroidogenesis and PI3K/AKT/mTOR Survival Signaling
    Article Snippet: For overexpression studies, the CDS of PRSS23 was amplified from Wuding chicken ovarian cDNA using gene-specific primers (Table S1) and subsequently cloned into the pMD-18T vector (TaKaRa). .. The insert was then excised by double digestion with Kpn I and Hind III, gel-purified, and ligated into the EGFP expression vector (Clontech Laboratories, Palo Alto, CA, USA). ..

    Plasmid Preparation:

    Article Title: Effects of TRIB3 gene overexpression and interference on lipid metabolism in mammary epithelial cells of yaks
    Article Snippet: The empty plasmid was extracted from the bacterial solution of pcDNA3.1 (+) plasmid (V79020, Invitrogen) stored in the laboratory using the High purity plasmid medium kit (EM101-01, full Gold) after amplification. .. The eukaryotic expression vector pcDNA3.1 (+) and purified PCR products were then digested with Hind III (1060S, TAKARA) and Xba I (1093S, TAKARA) restriction enzymes for 2 h at 37 °C. ..

    Article Title: Probiotic and antibacterial properties of recombinant Lactococcus lactis expressing the fusion antimicrobial peptides BMAP18-BSN37 in mice and chickens
    Article Snippet: .. Plasmid pNZ8148 was double-digested with Nco I and Hind III (Takara, Japan), and the linearized pNZ8148 plasmid was recovered by gel extraction. .. Homologous recombination of the Usp45-BMAP18-BSN37 gene with the linearized pNZ8148 plasmid was carried out using the ClonExpress II One Step Cloning Kit (Vazyme, China), resulting in the recombinant plasmid pNZ8148-Usp45-BMAP18-BSN37 (abbreviated as pUBB).

    Article Title: PfVPS4, an ESCRT AAA-ATPase, is essential for asexual proliferation and gametocyte sexual conversion in Plasmodium falciparum.
    Article Snippet: .. PCR products and the pET28a (+) vector were digested with BamHI and Hind III and ligated by T4 DNA ligase (Takara) with a molar ratio of 4:1 for insert to vector. ..

    Article Title: Tandem amplification of the umpA allele contributes to ceftazidime-avibactam heteroresistance in clinical carbapenem-resistant Klebsiella pneumoniae isolates
    Article Snippet: .. The vector pBAD33 was digested with Hind III or Sma I (Takara, Dalian, China), and the PCR products were then inserted behind the arabinose (Solarbio, Beijing, China)-inducible promoter for gene overexpression. ..

    Article Title: PRSS23 Promotes Ovarian Follicular Atresia in Wuding Chickens by Coordinately Suppressing Steroidogenesis and PI3K/AKT/mTOR Survival Signaling
    Article Snippet: For overexpression studies, the CDS of PRSS23 was amplified from Wuding chicken ovarian cDNA using gene-specific primers ( ) and subsequently cloned into the pMD-18T vector (TaKaRa). .. The insert was then excised by double digestion with Kpn I and Hind III, gel-purified, and ligated into the EGFP expression vector (Clontech Laboratories, Palo Alto, CA, USA). ..

    Article Title: PRSS23 Promotes Ovarian Follicular Atresia in Wuding Chickens by Coordinately Suppressing Steroidogenesis and PI3K/AKT/mTOR Survival Signaling
    Article Snippet: For overexpression studies, the CDS of PRSS23 was amplified from Wuding chicken ovarian cDNA using gene-specific primers (Table S1) and subsequently cloned into the pMD-18T vector (TaKaRa). .. The insert was then excised by double digestion with Kpn I and Hind III, gel-purified, and ligated into the EGFP expression vector (Clontech Laboratories, Palo Alto, CA, USA). ..

    Purification:

    Article Title: Effects of TRIB3 gene overexpression and interference on lipid metabolism in mammary epithelial cells of yaks
    Article Snippet: The empty plasmid was extracted from the bacterial solution of pcDNA3.1 (+) plasmid (V79020, Invitrogen) stored in the laboratory using the High purity plasmid medium kit (EM101-01, full Gold) after amplification. .. The eukaryotic expression vector pcDNA3.1 (+) and purified PCR products were then digested with Hind III (1060S, TAKARA) and Xba I (1093S, TAKARA) restriction enzymes for 2 h at 37 °C. ..

    Polymerase Chain Reaction:

    Article Title: Effects of TRIB3 gene overexpression and interference on lipid metabolism in mammary epithelial cells of yaks
    Article Snippet: The empty plasmid was extracted from the bacterial solution of pcDNA3.1 (+) plasmid (V79020, Invitrogen) stored in the laboratory using the High purity plasmid medium kit (EM101-01, full Gold) after amplification. .. The eukaryotic expression vector pcDNA3.1 (+) and purified PCR products were then digested with Hind III (1060S, TAKARA) and Xba I (1093S, TAKARA) restriction enzymes for 2 h at 37 °C. ..

    Article Title: PfVPS4, an ESCRT AAA-ATPase, is essential for asexual proliferation and gametocyte sexual conversion in Plasmodium falciparum.
    Article Snippet: .. PCR products and the pET28a (+) vector were digested with BamHI and Hind III and ligated by T4 DNA ligase (Takara) with a molar ratio of 4:1 for insert to vector. ..

    Article Title: Tandem amplification of the umpA allele contributes to ceftazidime-avibactam heteroresistance in clinical carbapenem-resistant Klebsiella pneumoniae isolates
    Article Snippet: .. The vector pBAD33 was digested with Hind III or Sma I (Takara, Dalian, China), and the PCR products were then inserted behind the arabinose (Solarbio, Beijing, China)-inducible promoter for gene overexpression. ..

    Gel Extraction:

    Article Title: Probiotic and antibacterial properties of recombinant Lactococcus lactis expressing the fusion antimicrobial peptides BMAP18-BSN37 in mice and chickens
    Article Snippet: .. Plasmid pNZ8148 was double-digested with Nco I and Hind III (Takara, Japan), and the linearized pNZ8148 plasmid was recovered by gel extraction. .. Homologous recombination of the Usp45-BMAP18-BSN37 gene with the linearized pNZ8148 plasmid was carried out using the ClonExpress II One Step Cloning Kit (Vazyme, China), resulting in the recombinant plasmid pNZ8148-Usp45-BMAP18-BSN37 (abbreviated as pUBB).

    Over Expression:

    Article Title: Tandem amplification of the umpA allele contributes to ceftazidime-avibactam heteroresistance in clinical carbapenem-resistant Klebsiella pneumoniae isolates
    Article Snippet: .. The vector pBAD33 was digested with Hind III or Sma I (Takara, Dalian, China), and the PCR products were then inserted behind the arabinose (Solarbio, Beijing, China)-inducible promoter for gene overexpression. ..

    DNA Ligation:

    Article Title: Polypeptide having esterification activity for L-menthol and/or hydrolyzing activity for L-menthol ester
    Article Snippet: A linker sequence (Nco I, Hind III) was added by PCR amplification (PrimeSTAR GXL DNA Polymerase (TaKaRa)), primer (forward primer: 5′-TTTTCCATGGCTCGTTCTATGCGTTCTCG-3′: SEQ ID NO: 6, reverse primer: 5′-AAAAAAGCTTAAACACCCGCCAGTTTCAGACGG-3′: SEQ ID NO: 7)) using the total synthesized structural gene (LipA; SEQ ID NO: 4) as a template, and then purification (NucleoSpin Gel and PCR Clean-up (MACHEREY-NAGEL)) was performed to obtain a gene fragment (BCL-LipA). .. The gene fragment (BCL-LipA) and pETDuet-1 (Novagen) were treated with a restriction enzyme (Nco I (TaKaRa), Hind III (TaKaRa)), then ligated (DNA Ligation Kit (TaKaRa)), and transformed into E. coli DH5a (TaKaRa) to obtain E. coli BCL-LipA. .. Plasmid extraction from E. coli BCL-LipA was performed using NucleoSpin Plasmid EasyPure (MACHEREY-NAGEL) after inoculating into LB Broth Base (invitrogen)+Amp: 100 μg/mL: 5 mL and shaking culture (37° C., 16 h, 140 rpm), thereby obtaining a plasmid (pETBCL-LipA).

    Transformation Assay:

    Article Title: Polypeptide having esterification activity for L-menthol and/or hydrolyzing activity for L-menthol ester
    Article Snippet: A linker sequence (Nco I, Hind III) was added by PCR amplification (PrimeSTAR GXL DNA Polymerase (TaKaRa)), primer (forward primer: 5′-TTTTCCATGGCTCGTTCTATGCGTTCTCG-3′: SEQ ID NO: 6, reverse primer: 5′-AAAAAAGCTTAAACACCCGCCAGTTTCAGACGG-3′: SEQ ID NO: 7)) using the total synthesized structural gene (LipA; SEQ ID NO: 4) as a template, and then purification (NucleoSpin Gel and PCR Clean-up (MACHEREY-NAGEL)) was performed to obtain a gene fragment (BCL-LipA). .. The gene fragment (BCL-LipA) and pETDuet-1 (Novagen) were treated with a restriction enzyme (Nco I (TaKaRa), Hind III (TaKaRa)), then ligated (DNA Ligation Kit (TaKaRa)), and transformed into E. coli DH5a (TaKaRa) to obtain E. coli BCL-LipA. .. Plasmid extraction from E. coli BCL-LipA was performed using NucleoSpin Plasmid EasyPure (MACHEREY-NAGEL) after inoculating into LB Broth Base (invitrogen)+Amp: 100 μg/mL: 5 mL and shaking culture (37° C., 16 h, 140 rpm), thereby obtaining a plasmid (pETBCL-LipA).



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