Taq Polymerase

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    Related websites

    Taq Polymerase - an overview | ScienceDirect Topics

    WEBTaq DNA Polymerase. Taq DNA polymerase is an 832-amino acid protein with an inferred molecular weight of 93,920 and a specific activity of 292,000 units/ mg; optimal polymerization activity is achieved at 75–80 ° C, with half-maximal activity at 60–70 ° C (Lawyer et al., 1993; see also Table 1). It's thermostability as measured as a half

    Sciencedirect.com


    Taq Polymerase - an overview | ScienceDirect Topics

    WEBDNA polymerase: It involves suitable thermostable DNA polymerases that could withstand temperature as high as 98°C. taq polymerase is the most commonly used polymerase, which is obtained from Thermus aquaticus bacteria whose natural habitat is hot springs. It has an optimum working temperature of 80°C.

    Sciencedirect.com


    Taq Polymerase - an overview | ScienceDirect Topics

    WEBtaq polymerase is a type of DNA polymerase enzyme commonly used in real-time PCR due to its robust activity and speed. It is known for its residual activity at low temperatures, which can lead to non-specific amplification, but 'hot-start' versions have been developed to inhibit its activity at low temperatures and prevent bias in the reaction.

    Sciencedirect.com


    Taq Polymerase - an overview | ScienceDirect Topics

    WEBApr 3, 2012 · The Polymerase Chain Reaction. W.T. Godbey, in An Introduction to Biotechnology, 2014 11.3 Extend. The extension step of traditional PCR is typically carried out using a DNA polymerase that was isolated from Thermus aquaticus (Taq), a heat-loving (thermophilic) bacterium that was first discovered in a hot spring associated with a …

    Sciencedirect.com


    A simple and efficient method for extraction of Taq DNA polymerase

    WEBSep 1, 2015 · Introduction. PCR is a most widely-used technique in biology, which utilizes thermostable DNA polymerase from Thermus aquaticus (Taq) [1], [2]. The gene that encoded the Taq DNA polymerase had been cloned and expressed in Escherichia coli efficiently [3]. This has greatly facilitated the production and reduced the price of the …

    Sciencedirect.com


    Bst polymerase — a humble relative of Taq polymerase

    WEBJan 1, 2023 · The biochemical characteristics of the two enzymes and Taq-polymerase were also compared (Table 1). The specific activity, k cat, and processivity of Bst polymerase were significantly higher than those of Taq-polymerase and KF. At the same time, The K M values for DNA and dNTP were closer across the different enzymes.

    Sciencedirect.com


    A simple and efficient method for Taq DNA polymerase …

    WEBApr 1, 2023 · In order to compare the activity of our purified Taq DNA polymerases with the activity of Taq DNA polymerase within the TaqMan Gene Expression Master Mix (Applied Biosystems), the lab purified polymerases were added to the commercial master mix previously depleted from the commercial Taq DNA polymerase using a filter of 50KDa …

    Sciencedirect.com


    TA Cloning - an overview | ScienceDirect Topics

    WEBTaq DNA polymerase exhibits a very useful habit of adding an extra nucleotide, most often an A, at the 3′ end of each strand of the product that it generated. This is the basis for a convenient method known as TA cloning , in which the investigator anneals and then ligates the Taq A-tailed product into a vector that exhibits a 3′“T over-hang” on each strand ( …

    Sciencedirect.com


    PCR enhancers: Types, mechanisms, and applications in long …

    WEBJun 1, 2022 · 2. The essential ingredients of long- and short-range PCRs. PCR is performed in a buffered reaction mixture consisting of a pair of primers, template DNA, DNA polymerase, magnesium (Mg 2+) ions, and deoxyribonucleoside triphosphates (dNTPs). The buffer maintains the pH of the reaction mixture and supplies potassium (K +) or …

    Sciencedirect.com


    Thermally reversible inactivation of Taq polymerase in an organic

    WEBMay 16, 2005 · taq polymerase was eluted from the column with a 0–4 M gradient of urea over 9 column volumes. Fractions containing taq polymerase were pooled and concentrated/dialysed to remove traces of urea using a Vivaflow 50 system (Vivascience AG, Germany) and buffer containing 25 mM Tris–HCl (pH 7.5) and 1 mM EDTA and the …

    Sciencedirect.com


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