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Phanta UC Super-Fidelity DNA Polymerase for Library Amplification

NGS Library Prep kits

Molecular Research

Drug Discovery

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Number of views:
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Phanta UC Super-Fidelity DNA Polymerase for Library Amplification

Phanta® Uc Super-Fidelity DNA Polymerase is a new generation of high-fidelity DNA polymerase modified from Pfu DNA Polymerase, with extremely high amplification efficiency Rate and wide template adaptability. Compared with Pfu DNA Polymerase, Phanta® Uc Super-Fidelity DNA Polymerase has greatly improved its mobility. Even very complex templates can complete PCR reactions quickly and accurately. Its mismatch rate is 1/52 of Taq DNA Polymerase and 1/6 of Pfu DNA Polymerase, and it completely overcomes the inability of conventional high-fidelity enzymes to use dUTP as raw material for polymerization, the inability to use amplification primers containing dUTP, and the inability to use DNA containing dUTP is used as an amplification template and many other disadvantages. With a carefully optimized reaction buffer for library amplification, Phanta® Uc Super-Fidelity DNA Polymerase for Library Amplification can achieve high-throughput measurement The low preference, high efficiency and high stability amplification of sequence library. The amplified product is blunt-ended and can be directly used for blunt-ended cloning.    Gap filling (no chain displacement activity); Cut off the 3'protruding end or fill in the 5'protruding end to form a flat end   All components stored at -20°C
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71.0
Market price
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71.0
Number of views:
2556
Product serial number
P507-01/02
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Phanta® Uc Super-Fidelity DNA Polymerase is a new generation of high-fidelity DNA polymerase modified from Pfu DNA Polymerase, with extremely high amplification efficiency
Rate and wide template adaptability. Compared with Pfu DNA Polymerase, Phanta® Uc Super-Fidelity DNA Polymerase has greatly improved its mobility. Even very complex templates can complete PCR reactions quickly and accurately. Its mismatch rate is 1/52 of Taq DNA Polymerase and 1/6 of Pfu DNA Polymerase, and it completely overcomes the inability of conventional high-fidelity enzymes to use dUTP as raw material for polymerization, the inability to use amplification primers containing dUTP, and the inability to use DNA containing dUTP is used as an amplification template and many other disadvantages. With a carefully optimized reaction buffer for library amplification, Phanta® Uc Super-Fidelity DNA Polymerase for Library Amplification can achieve high-throughput measurement
The low preference, high efficiency and high stability amplification of sequence library. The amplified product is blunt-ended and can be directly used for blunt-ended cloning. 

 

Gap filling (no chain displacement activity);
Cut off the 3'protruding end or fill in the 5'protruding end to form a flat end

 

All components stored at -20°C

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amplification
dna
polymerase
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