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minibest plasmid purification kit  (TaKaRa)


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    TaKaRa minibest plasmid purification kit
    Minibest Plasmid Purification Kit, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 462 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/minibest+plasmid+purification+kit+ver/TaKaRa+MiniBEST+Plasmid+Purification+Kit+Ver%2E4%2E0/pm42103278-166-22-26
    Average 96 stars, based on 462 article reviews
    minibest plasmid purification kit - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Expressing:

    Article Title: Recombinant varicella-zoster virus (VZV) vaccine
    Article Snippet: .. Construction of Expression Plasmids Carrying the VZV gE-Fc Gene A glycerol-preserved strain with the recombinant gene provided by the Nanjing Genscript Biotechnology Co., Ltd was inoculated into an LB (Amp+) medium and cultivated at 37° C. and 180 rpm for 15 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Recombinant:

    Article Title: Recombinant varicella-zoster virus (VZV) vaccine
    Article Snippet: .. Construction of Expression Plasmids Carrying the VZV gE-Fc Gene A glycerol-preserved strain with the recombinant gene provided by the Nanjing Genscript Biotechnology Co., Ltd was inoculated into an LB (Amp+) medium and cultivated at 37° C. and 180 rpm for 15 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Plasmid Preparation:

    Article Title: Recombinant varicella-zoster virus (VZV) vaccine
    Article Snippet: .. Construction of Expression Plasmids Carrying the VZV gE-Fc Gene A glycerol-preserved strain with the recombinant gene provided by the Nanjing Genscript Biotechnology Co., Ltd was inoculated into an LB (Amp+) medium and cultivated at 37° C. and 180 rpm for 15 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Genetically engineered strain
    Article Snippet: .. Finally, the correct transformants were preserved, and the following plasmids were obtained: pRSFDuet-cmaao-pmkdc, pRSFDuet-cmaao-Ilkdc, pRSFDuet-pmaao-pmkdc and pRSFDuet-pmaao-Ilkdc containing L-amino acid oxidase genes and α-keto acid decarboxylase genes. pETDuet-ecadh1-kpfdh, pETDuet-ecadh1-bsgdh, pETDuet-ecadh1-papdh, pETDuet-ecadh2-kpfdh, pETDuet-ecadh2-bsgdh and pETDuet-ecadh2-Papdh containing alcohol dehydrogenase genes and enzyme genes capable of reducing NAD(P). (5) Construction of pRSFDuet-1 and pETDuet-1 Double Plasmid Four Genes Co-Expressed System According to the instructions for use provided by the manufacturer, pRSFDuet-cmaao-pmkdc, pRSFDuet-cmaao-Ilkdc, pRSFDuet-pmaao-pmkdc, pRSFDuet-pmaao-Ilkdc plasmid DNA1 and pETDuet-ecadh1-kpfdh, pETDuet-ecadh1-bsgdh, pETDuet-ecadh1-papdh, pETDuet-ecadh2-kpfdh, pETDuet-ecadh2-bsgdh, pETDuet-ecadh2-papdh plasmid DNA2 obtained in step (4) were extracted with TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Elevated and atmospheric‐level methane consumption by soil methanotrophs of three grasslands in China
    Article Snippet: .. Plasmid DNA, used for calibration, was prepared using the pEASYT1 Cloning Kit (Beijing TransGen Biotech Co., Ltd.) and the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (TaKaRa Bio Inc.) containing a cloned target gene according to the manufacturer's instructions.

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Article Title: Trophic status strongly regulates nitrous oxide but not methane production in global freshwater lake sediments
    Article Snippet: .. The positive colonies were then selected for plasmid extraction using the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (Takara Bio, Shiga, Japan).

    Article Title: Photolysis of methicillin-resistant Staphylococcus aureus using Cu-doped carbon spheres.
    Article Snippet: PAPER Soo Hyun Kim et al. Biodegradable vascular stents with high tensile and compressive strength, a novel strategy for applying monofilaments via solid-state drawing and shaped-annealing processes Volume 5 Number 3 March 2017 Pages 343-602 Biomaterials Science This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication.

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Changes in the activities of key enzymes and the abundance of functional genes involved in nitrogen transformation in rice rhizosphere soil under different aerated conditions
    Article Snippet: All qPCR reactions were carried out on an MG96+ real-time PCR machine (Hangzhou Langji Scientific Instrument Co., Ltd., China) in wells containing 10 μL of SYBR@ Premix ExTaq (TaKaRa, Japan), including 0.8 μL forward primer (5 μmol L–1), 0.8 μL reverse primer (5 μmol L–1), 7.4 μL double deionizedwater (ddH2O), and 1 μL template DNA adjusted to a final volume of 20 μL with ddH2O. .. Plasmids for qPCR were extracted using a TaKaRa MiniBEST Plasmid Purification Kit ver. .. 4.0 (TaKaRa, Japan), and then the purified PCR products were cloned into the Pgem-T Easy Vector (Promega, Madison, WI, USA) and transformed into Escherichia coli JM109 competent cells (Promega, Madison, WI, USA).

    Purification:

    Article Title: Recombinant varicella-zoster virus (VZV) vaccine
    Article Snippet: .. Construction of Expression Plasmids Carrying the VZV gE-Fc Gene A glycerol-preserved strain with the recombinant gene provided by the Nanjing Genscript Biotechnology Co., Ltd was inoculated into an LB (Amp+) medium and cultivated at 37° C. and 180 rpm for 15 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Genetically engineered strain
    Article Snippet: .. Finally, the correct transformants were preserved, and the following plasmids were obtained: pRSFDuet-cmaao-pmkdc, pRSFDuet-cmaao-Ilkdc, pRSFDuet-pmaao-pmkdc and pRSFDuet-pmaao-Ilkdc containing L-amino acid oxidase genes and α-keto acid decarboxylase genes. pETDuet-ecadh1-kpfdh, pETDuet-ecadh1-bsgdh, pETDuet-ecadh1-papdh, pETDuet-ecadh2-kpfdh, pETDuet-ecadh2-bsgdh and pETDuet-ecadh2-Papdh containing alcohol dehydrogenase genes and enzyme genes capable of reducing NAD(P). (5) Construction of pRSFDuet-1 and pETDuet-1 Double Plasmid Four Genes Co-Expressed System According to the instructions for use provided by the manufacturer, pRSFDuet-cmaao-pmkdc, pRSFDuet-cmaao-Ilkdc, pRSFDuet-pmaao-pmkdc, pRSFDuet-pmaao-Ilkdc plasmid DNA1 and pETDuet-ecadh1-kpfdh, pETDuet-ecadh1-bsgdh, pETDuet-ecadh1-papdh, pETDuet-ecadh2-kpfdh, pETDuet-ecadh2-bsgdh, pETDuet-ecadh2-papdh plasmid DNA2 obtained in step (4) were extracted with TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Elevated and atmospheric‐level methane consumption by soil methanotrophs of three grasslands in China
    Article Snippet: .. Plasmid DNA, used for calibration, was prepared using the pEASYT1 Cloning Kit (Beijing TransGen Biotech Co., Ltd.) and the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (TaKaRa Bio Inc.) containing a cloned target gene according to the manufacturer's instructions.

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Article Title: Trophic status strongly regulates nitrous oxide but not methane production in global freshwater lake sediments
    Article Snippet: .. The positive colonies were then selected for plasmid extraction using the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (Takara Bio, Shiga, Japan).

    Article Title: Photolysis of methicillin-resistant Staphylococcus aureus using Cu-doped carbon spheres.
    Article Snippet: PAPER Soo Hyun Kim et al. Biodegradable vascular stents with high tensile and compressive strength, a novel strategy for applying monofilaments via solid-state drawing and shaped-annealing processes Volume 5 Number 3 March 2017 Pages 343-602 Biomaterials Science This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication.

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Article Title: Changes in the activities of key enzymes and the abundance of functional genes involved in nitrogen transformation in rice rhizosphere soil under different aerated conditions
    Article Snippet: All qPCR reactions were carried out on an MG96+ real-time PCR machine (Hangzhou Langji Scientific Instrument Co., Ltd., China) in wells containing 10 μL of SYBR@ Premix ExTaq (TaKaRa, Japan), including 0.8 μL forward primer (5 μmol L–1), 0.8 μL reverse primer (5 μmol L–1), 7.4 μL double deionizedwater (ddH2O), and 1 μL template DNA adjusted to a final volume of 20 μL with ddH2O. .. Plasmids for qPCR were extracted using a TaKaRa MiniBEST Plasmid Purification Kit ver. .. 4.0 (TaKaRa, Japan), and then the purified PCR products were cloned into the Pgem-T Easy Vector (Promega, Madison, WI, USA) and transformed into Escherichia coli JM109 competent cells (Promega, Madison, WI, USA).

    Cloning:

    Article Title: Elevated and atmospheric‐level methane consumption by soil methanotrophs of three grasslands in China
    Article Snippet: .. Plasmid DNA, used for calibration, was prepared using the pEASYT1 Cloning Kit (Beijing TransGen Biotech Co., Ltd.) and the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (TaKaRa Bio Inc.) containing a cloned target gene according to the manufacturer's instructions.

    Polymerase Chain Reaction:

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Amplification:

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Agarose Gel Electrophoresis:

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Electrophoresis:

    Article Title: Candidatus Liberibacter asiaticus: An important factor affecting bacterial community composition and Wolbachia titers in Asian citrus psyllid
    Article Snippet: .. The TaKaRa MiniBEST Plasmid Purification Kit Ver (TaKaRa, Kusatsu, Japan) was used to extract plasmids that would be subjected to PCR amplification using the specific primer sets developed for Wolbachia in a thermocycler set at 10 min at 95°C, followed by 20s at 95°C and 1 min at 60°C (35 cycles), followed by insert size verification on a 1% agarose gel under electrophoresis. ..

    Extraction:

    Article Title: Trophic status strongly regulates nitrous oxide but not methane production in global freshwater lake sediments
    Article Snippet: .. The positive colonies were then selected for plasmid extraction using the TaKaRa MiniBEST Plasmid Purification Kit Ver. .. 4.0 (Takara Bio, Shiga, Japan).

    DNA Extraction:

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Construct:

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Transformation Assay:

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Incubation:

    Article Title: Multiplex digital PCR: a superior technique to qPCR for the simultaneous detection of duck Tembusu virus, duck circovirus, and new duck reovirus
    Article Snippet: .. PCR amplification was performed with DTMUV, DuCV, NDRV cDNA, or DNA as a template using three pairs of specific primers, and the PCR products were purified by applying the TaKaRa MiniBEST Agarose Gel DNA Extraction Kit Ver.4.0 (Dalian, China) and ligated into the pMDTM18-T Vector (China); the constructs were transformed into E. coli DH5α competent cells, coated and incubated at 37°C for 16 h, and the TaKaRa MiniBEST Plasmid Purification Kit Ver. ..

    Real-time Polymerase Chain Reaction:

    Article Title: Changes in the activities of key enzymes and the abundance of functional genes involved in nitrogen transformation in rice rhizosphere soil under different aerated conditions
    Article Snippet: All qPCR reactions were carried out on an MG96+ real-time PCR machine (Hangzhou Langji Scientific Instrument Co., Ltd., China) in wells containing 10 μL of SYBR@ Premix ExTaq (TaKaRa, Japan), including 0.8 μL forward primer (5 μmol L–1), 0.8 μL reverse primer (5 μmol L–1), 7.4 μL double deionizedwater (ddH2O), and 1 μL template DNA adjusted to a final volume of 20 μL with ddH2O. .. Plasmids for qPCR were extracted using a TaKaRa MiniBEST Plasmid Purification Kit ver. .. 4.0 (TaKaRa, Japan), and then the purified PCR products were cloned into the Pgem-T Easy Vector (Promega, Madison, WI, USA) and transformed into Escherichia coli JM109 competent cells (Promega, Madison, WI, USA).



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