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ex taq dna polymerase  (TaKaRa)


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    Structured Review

    TaKaRa ex taq dna polymerase
    Ex Taq Dna Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 98/100, based on 15987 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dna+polymerase/TaKaRa+Ex+Taq+DNA+Polymerase/pmc13090712-41-0-7
    Average 98 stars, based on 15987 article reviews
    ex taq dna polymerase - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    other:

    Article Title: Engineering a robust IsPETase for energy-efficient PET depolymerization in natural seawater at ambient temperatures.
    Article Snippet: Escherichia coli (E. coli) DH5α competent cells, E. coli BL21 (DE3) competent cells and DNA polymerase were obtained from Takara (Dalian, China).

    Article Title: Engineering a Tyrosol-Responsive Dynamic System in Saccharomyces cerevisiae for Adaptive Regulation of Hydroxytyrosol Biosynthesis.
    Article Snippet: Static metabolic regulation during microbial synthesis of polyphenolic compounds leads to tyrosol accumulation, inducing cellular toxicity and growth inhibition.. Dynamic regulation effectively alleviates the imbalance between cell growth and production; yet, a tyrosol-responsive dynamic system for yeast adaptive regulation remains unreported.. In this study, endogenous tyrosol-responsive promoters were mined via transcriptomics, and the optimal promoter PYOR153W was identified.

    Article Title: Engineering a robust Is PETase for energy-efficient PET depolymerization in natural seawater at ambient temperatures
    Article Snippet: Escherichia coli ( E. coli ) DH5α competent cells, E. coli BL21 (DE3) competent cells and DNA polymerase were obtained from Takara (Dalian, China).

    Polymerase Chain Reaction:

    Article Title: Lung fibrosis model and methods of using the same
    Article Snippet: .. The DNA polymerase for the pre-amplification step (one cycle of 95° C. for 3 min; 15-17 cycles of 98° C. for 15 s, 65° C. for 30 s and 68° C. for 4 min; and one cycle of 72° C. for 10 min) was replaced by Terra PCR direct polymerase (Takara, 639271). ..

    Plasmid Preparation:

    Article Title: Engineering Precursor and NADPH Supply to Enhance 1,4-Butanediol Production in Plasmid-Free Escherichia coli .
    Article Snippet: 1,4-Butanediol (1,4-BDO) is an important non-natural platform chemical for biodegradable plastics, yet its microbial production is constrained by inadequate NADPH availability.. In this study, five heterologous enzymes were introduced into Escherichia coli for the biosynthesis of 1,4-BDO.. Through coordinated regulation of pathway enzyme expression and enhancement of key rate-limiting steps, a 1,4-BDO titer of 0.93 g/L was achieved from glucose.

    Extraction:

    Article Title: Engineering Precursor and NADPH Supply to Enhance 1,4-Butanediol Production in Plasmid-Free Escherichia coli .
    Article Snippet: 1,4-Butanediol (1,4-BDO) is an important non-natural platform chemical for biodegradable plastics, yet its microbial production is constrained by inadequate NADPH availability.. In this study, five heterologous enzymes were introduced into Escherichia coli for the biosynthesis of 1,4-BDO.. Through coordinated regulation of pathway enzyme expression and enhancement of key rate-limiting steps, a 1,4-BDO titer of 0.93 g/L was achieved from glucose.

    Gel Purification:

    Article Title: Engineering Precursor and NADPH Supply to Enhance 1,4-Butanediol Production in Plasmid-Free Escherichia coli .
    Article Snippet: 1,4-Butanediol (1,4-BDO) is an important non-natural platform chemical for biodegradable plastics, yet its microbial production is constrained by inadequate NADPH availability.. In this study, five heterologous enzymes were introduced into Escherichia coli for the biosynthesis of 1,4-BDO.. Through coordinated regulation of pathway enzyme expression and enhancement of key rate-limiting steps, a 1,4-BDO titer of 0.93 g/L was achieved from glucose.



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