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BioMaster LR HS-PCR (2x)

Features: 2× reaction mix is developed for hot-start amplification of long DNA fragments ranging from 0.2 to 30 kbp, GC-rich (>65%) and complicated regions of DNA.

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BioMaster LR HS-PCR (2×) includes 2× BioMaster LR HS-PCR (2×) reaction mix, sterile water and 6× loading buffer. The master mix is developed for amplification of long (0.2 through 30 kbp) DNA fragments with enhanced specificity, high fidelity and reaction yield. The mix is also ideally suitable for amplification of GC-rich (>65%) and complicated DNA regions. BioMaster LR HS-PCR (2×) contains all components necessary for PCR (except for DNA template and primers): polymerase mix (HS-Taq and Pfu), deoxynucleoside triphosphate mix, PCR buffer, and Mg2+.
BioMaster LR HS-PCR (2×) mix contains a combination of two highly purified enzymes: highly processive HS-Taq DNA polymerase and Pfu DNA polymerase with correction function. The mixture of polymerases is inactive at room temperature (hot start), and their activation requires preheating of the reaction solution at 95 °C for 5 min.
The combination of polymerases enables to enhance fidelity and reliability of amplification reaction several fold compared to PCR with Taq polymerase only. Synergic performance of the two enzymes allows to obtain PCR products up to 30 kbp. The products obtained using BioMaster LR HS-PCR (2×) mostly contain 3´-dA ends. Hence, they can be further used for cloning.
The buffer is optimized for efficient performance of both polymerases and provides high reaction yield. Use of the kit helps saving time and minimizes contamination risk due to reduced number of pipetting steps.
Area of application:
  • Long-range PCR
  • Product generation for TA-cloning
  • Amplification of GC-rich and complicated templates
Product features:
  • Optimized for specific performance of Taq and Pfu DNA polymerases;
  • Composition of the mixture allows long-term storage (the storage of BioMaster LR HS-PCR (2×) at room temperature for 7 days does not affect PCR efficiency) and multiple thawing-freezing cycles (more than 50 times)
Benefits of use:
  • Amplification of long fragments:
up to 30 kbp (viral DNA templates)
up to 15 kbp (genomic DNA templates)
  • Enhanced amplification fidelity compared to that performed using Taq DNA polymerase only
  • Hot-start enzyme increases specificity, sensitivity and reaction yield
  • Activation of HS-Taq DNA polymerase takes not more than 5 min
  • Amplification of a wide spectrum of DNA templates
  • PCR products can be further subjected to TA cloning due to the presence of deoxyadenosine overhangs in amplified DNA
 
Storage and transportation: at -20 °С; not more than 50 thawing-freezing cycles.
 
Storage terms: 1 year (under proper storage and transportation conditions).