BioMaster HS-qPCR (2×)

BioMaster HS-qPCR (2×)
Master mix containing Hot-Start Taq DNA polymerase for real-time PCR with fluorescent probes

Price: 50.00 EUR
Not in stock

BioMaster HS-qPCR (2×) contains 2× BioMaster HS-qPCR reaction mix and sterile water. The kit was developed for quantitative real-time PCR with fluorescently labeled probes. The mix contains all components, besides DNA template, primers and probe, needed for a PCR with fluorescently labeled probes: HS-Taq DNA polymerase, dNTPs mixture, 2× PCR buffer and Mg2+.

The master mix is optimized for  efficient and reproducible hot-start real-time PCR of genomic, plasmid and viral DNA samples. The mix contains additional components increasing stability of HS-Taq DNA polymerase during the reaction. BioMaster HS-qPCR (2×) includes components that influence primer annealing temperature and characteristics of template melting thus enabling to increase PCR specificity and use templates with complicated spatial structure. 

DNA polymerase included in the kit is inactive at room temperature and requires preheating at 95 °C for 5 min. Use of the kit saves time and minimizes the risk of contamination due to reduced number of pipetting steps.

Kit content:
  • 100 mM Tris-HCl (рН 8.5 at 25 °С)
  • 100 mM KCl
  • dNTPs (0.4 mM each)  
  • 10 mM MgCl2
  • 0.1 U/µl Taq DNA polymerase
  • 0.025% Tween 20
  • stabilizers of HSTaq DNA polymerase
  • Hot-start real-time PCR with fluorescently-labeled probes
  • Conventional PCR
  • High-throughput PCR
  • Multiplex PCR
  • Genotyping
Long term storage at -20 °С. Can be shipped at ambient temperature. Avoid repetitive freeze-thaw cycles.
Copyright MAXXmarketing GmbH
JoomShopping Download & Support

We use cookies on our website. Some of them are essential for the operation of the site, while others help us to improve this site and the user experience (tracking cookies). You can decide for yourself whether you want to allow cookies or not. Please note that if you reject them, you may not be able to use all the functionalities of the site.