DNA Polymerases
New England Biolabs, Inc. Q5U™ Hot Start High-Fidelity DNA Polymerase – 500 units
Q5U Hot Start High-Fidelity DNA Polymerase is a modified version of Q5 High-Fidelity DNA Polymerase, a novel thermostable DNA polymerase that possesses 3' to 5' exonuclease activity, and is fused to a processivity-enhancing Sso7d domain. Q5U contains a mutation in the uracil-binding pocket that enables the ability to read and amplify templates containing uracil and inosine bases.
Sigma Aldrich Fine Chemicals Biosciences Taq DNA Polymerase dNTPack
Taq DNA Polymerase is a highly processive 5-3 DNA polymerase that lacks 3-5 exonuclease activity. It is a single polypeptide chain with a molecular weight of approximately 95 kDa.Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM a strain lacking Taq I restriction endonuclease. The enzyme preparation obtained from E.coli is free of nonspecific engo- or exonucleases according to the current quality control procedures.
Sigma Aldrich Fine Chemicals Biosciences Taq DNA Polymerase dNTPack
Taq DNA Polymerase is a highly processive 5-3 DNA polymerase that lacks 3-5 exonuclease activity. It is a single polypeptide chain with a molecular weight of approximately 95 kDa.Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM a strain lacking Taq I restriction endonuclease. The enzyme preparation obtained from E.coli is free of nonspecific engo- or exonucleases according to the current quality control procedures.
Sigma Aldrich Fine Chemicals Biosciences Taq DNA Polymerase 5 U/mul
Taq DNA Polymerase is a highly processive 5-3 DNA polymerase that lacks 3-5 exonuclease activity. It is a single polypeptide chain with a molecular weight of approximately 95 kDa.Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM a strain lacking Taq I restriction endonuclease. The enzyme was cloned in E.coli.
Sigma Aldrich Fine Chemicals Biosciences Taq DNA Polymerase dNTPack
Taq DNA Polymerase is a highly processive 5-3 DNA polymerase that lacks 3-5 exonuclease activity. It is a single polypeptide chain with a molecular weight of approximately 95 kDa.Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM a strain lacking Taq I restriction endonuclease. The enzyme preparation obtained from E.coli is free of nonspecific engo- or exonucleases according to the current quality control procedures.
Sigma Aldrich Fine Chemicals Biosciences fastStartTM Taq DNA Polyme
The enzyme dNTPack comprises fastStart Taq DNA Polymerase and a ready-to-use SOLUTIONon of PCR grade nucleotides. fastStart Taq DNA Polymerase is a versatile enzyme that can be used in a wide variety of applications and on multiple instrument platforms. This modified thermostable recombinant Taq DNA polymerase is inactive at temperatures below 75 C but is activated by a 2 to 4 minute heat activation step at 95 C. Since it is inactive at low temperatures fastStart Taq DNA Polymerase cannot elongate non-specific primer-template hybrids that may form at those temperatures. An optimized PCR buffer system and a GC-RICH SOLUTIONon to enable the enzyme to handle a wide range of templates are also supplied.
Biotang Inc Pfu-DNA Polymerase Recombinant, Source Escherichia Coli. Pfu DNA Polymerase is a thermo-stable enzyme having a Mw of about 90kDa.
Pfu-DNA Polymerase Recombinant, Source Escherichia Coli. Pfu DNA Polymerase is a thermo-stable enzyme having a Mw of about 90kDa.
Genscript Corporation 10 x iTaq/i Buffer
The 10 x i Taq /i Buffer contains 500 mM KCl 100 mM Tris HCl (pH 9 0 at 25 C) 15 mM MgCl sub 2 /sub and 1% Triton X-100 This buffer is optimized for use with 200 M dNTPs
Genscript Corporation Hot Start Taq DNA Polymerase
Hot Start Taq DNA Polymerase is a recombinant thermostable Taq DNA polymerase complexed with a thermolabile neutralizing antibody that blocks the polymerase activity prior to the initial DNA denaturation step of PCR When the temperature of the PCR reaction mix reaches 95 C during the initial DNA denaturing step of PCR cycling activity of the Taq DNA polymerase is fully restored br/