• Use in cloning, mutagenesis or DNA chip • 50 times more accurate than a standard TAQ Polymerase • Elongation rate: 2kb / min for eukaryotic genomic DNA or cDNAs • Between 0.5 and 1 U of DNA polymerase required for 25 µl of reaction mixture • 5X reaction buffer with additives improving the activity and the reaction rate of the enzyme • Storage 12 months at -20 ° C
• Mixture of DNA polymerase Pfu (Pyrococcus furiosus) and a thermostable polymerization activator • Ultrapure, thermostable and proofreading recombinant polymerase • Formulation designed to synthesize DNA sequences up to 20 kb • More than 10 times more accuracy than a standard Taq • Recommended for high-fidelity PCR, GC-rich sequences or sequences with problematic secondary structures, directed mutagenesis and blunt end cloning • Can also be used for conventional PCR and high temperature primer extension • Supplied with a 10X reaction buffer • Available in 100, 500 and 2500 unit formats • OnPfuPlus! DNA polymerase: hot start version, stable at room temperature, activation in 10 min at 90 °C
• Optimized mixture of thermostable DNA polymerases Taq (Thermus aquaticus), Pfu (Pyrococcus furiosus) and a polymerization activator • Ultra-pure, thermostable recombinant polymerases. Pfu proofreading. • Unique composition of the reaction buffer promoting pH stability at high temperature and ensuring high efficiency for long sequence amplifications • Amplification of genomic DNA sequences from 3 to 25 kb and episomal DNA sequences up to 40 kb • Particularly suitable for the amplification of eukaryotic genomes • Ideal for genome mapping and sequencing of long fragments • Supplied with a 10X reaction buffer • Available in 100 and 500 unit formats
• Optimized mixture of thermostable DNA polymerases Taq (Thermus aquaticus), Pfu (Pyrococcus furiosus) and a polymerization activator • Ultrapure recombinant polymerases, thermostable and hot start. Pfu proofreading • The hot start property of the polymerases makes them inactive at room temperature allowing the preparation of the reaction mix at room temperature • Unique composition of the reaction buffer promoting pH stability at high temperature and ensuring high efficiency for long sequence amplifications • Amplification of genomic DNA sequences from 3 to 25 kb and episomal DNA sequences up to 40 kb • Particularly suitable for the amplification of eukaryotic genomes • Ideal for genome mapping and sequencing of long fragments • Supplied with a 10X reaction buffer • Available in 100 and 500 unit formats
• Fast expansion: up to 1 kb in 15 seconds • 100 times more accurate than native Taq polymerase • 2X formulation for high inhibitor tolerance • Optimised buffers with additives to improve PCR and increase sensitivity at low copy numbers • Generates clean ends • Ideal for cloning, mutagenesis, sequencing