• 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
• For amplification in fast PCR mode, reduces the time of a PCR cycle by up to 4 times compared to a standard protocol. • Elongation step 3 to 4 times faster than with conventional DNA polymerase • Hot start enzyme inactivated at room temperature, activation in only 30 seconds at 98 °C • For the amplification of Low complexity DNA fragments (cDNA, lambda, plasmid DNA) up to 5 kb or up to 3 kb for human, animal or plant DNA • Ready-to-use mix Kit; requires only the matrix, primers and molecular biology quality water • Available in a 'Ready to load' version for direct deposit on gel, contains a load buffer and two dyes for migration monitoring (blue (3,5-4,5 kb) and yellow (35-45 pb)) • Available in a version with UNG to reduce the risk of cross-contamination • Stable 30 days at room temperature, long-term storage at -20 °C
• Mix for quantitative PCR with fast protocol, elongation 3 to 4 times faster than with conventional DNA polymerase • Hot start enzyme inactivated at room temperature, activation in only 30 seconds at 95 °C • qPCR results obtained in only 30 minutes depending on thermocycler performance (optimized for qPCR Mic thermocyclers (Cat No. 634001 and 634002) • Mix also available with ROX or PURPLE dye for thermocyclers requiring a reference signal for data normalization. • Stable 30 days at room temperature, long-term storage at -20 °C
• For the stabilization of DNA, RNA or circulating, cell-free DNA (ccfDNA) depending on Cat.No. • Secure and standardized sampling • CE/IVD certified • Compatible with sensitive applications: RT-qPCR, NGS, methylation...
• DNA polymerase hot start at an initial concentration of 2.5 U/µl • Increases PCR specificity, sensitivity and throughput by reducing the risk of mismatch and primer-dimer formation • Activated during the initial 10 min denaturation step at 95 °C • Conserved 5'-'3' exonuclease activity and absence of 3'-'5' exonuclease activity • Adds a free adenine to the 3' end of the amplicon (monoadenylation) • Kit with 3 different 10X reaction buffers: without MgCl2 (A), with MgCl2 (B), with 2 inert dyes for direct deposit (C) • Kit supplied with dNTPs (separate tube)
• DNA polymerase Taq hot start • Hot start system by aptamer technology: reversible activation / inactivation • Polymerase inactivated below 45 °C • Fully activated polymerase above 60 °C • No specific activation step required as with antibody technology • Ideal for rapid PCR, routine PCR and SNP analysis in particular
• Fast qPCR mix with SYBR Green I dye for use with most real-time thermal cyclers • Contains Perpetual Taq hot start DNA polymerase, optimised buffer, dNTPs (dTTP partially replaced by dUTP) and SYBR Green I dye • Uracile N-glycosylase (UNG) heat-labile provided to limit the risk of cross-contamination (optional use) • Available with ROX dye (separate tube) for standardisation
• Fast qPCR mix with hydrolysis probes for use with most real-time thermal cyclers • Contains Perpetual Taq hot start DNA polymerase, optimised buffer, dNTPs (dTTP partially replaced by dUTP) and SYBR Green I dye • Uracile N-glycosylase (UNG) heat-labile provided to limit the risk of cross-contamination (optional use) • Available with ROX dye (separate tube) for standardisation
• Mix designed for high resolution melting curve (HRM) analysis of DNA samples • Allows detection of gene mutations and single polymorphisms (SNPs) including class III and IV • Contains onTaq hot start DNA polymerase, optimised buffer, dNTPs and fluorescent dye • OnTaq polymerase activated during the initial denaturation step of the PCR at 95 °C for 15 min