gb Elite PCR Master Mix

gb Elite PCR Master Mix is intended for research PCR and real-time PCR applications with fluorescently labelled probes and with high sensitivity and efficiency request. Beneficial feature is its enhanced resistance to PCR inhibitors. It is not intended for use in diagnostics.

Description of the product

gb Elite PCR Master Mix consists of hot-start Taq DNA polymerase, reaction buffer, dNTP, MgCl2 and additives that prevent PCR inhibition. Taq polymerase is chemically modified DNA polymerase from Thermus aquaticus. This polymerase is completely inactive at room temperature but it is rapidly activated during the initial denaturation step of PCR.

Parameters of the product

  • Master Mix is a 2× concentrated solution.
  • It contains all the components necessary for PCR performance.
  • It is specified especially for real-time PCR applications demanding high sensitivity, for example microbial DNA detection and somatic mutations detection.
  • Master Mix is enriched with components which prevent PCR reaction inhibition through which higher reliability of the detection is ensured.
  • Polymerase is a hot-start type with a short activation time (3 min / 95 °C), with 5´-3´ polymerase and exonuclease activity, 3´-5´ exonuclease activity is not present.


gb PCR Master Mix by application
gb Elite
end-point PCR, common PCR amplification
real-time PCR without probes
real-time PCR with hydrolysis probes

real-time PCR with LNA probes
real-time PCR with hybridization probes
real-time PCR with High Resolution Melting Analysis
real-time PCR with low DNA samples

real-time PCR with inhibited sampels

Cat. No. Product No. of reactions Price
3008 gb Elite PCR Master Mix 100
Add to Quote

1 tube contains reagents to provide 100 PCR reactions (20 μl volume of each reaction).

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gb OneStep RT-qPCR Kit is intended for reverse transcription (RT) and real-time PCR (qPCR) performed in one step (in one reaction), i.e. onestep RT-qPCR. No additional instrumentation is required; the onestep RT-qPCR analysis can be performed directly on any real-time PCR cycler simply by adding a thermal step for reverse transcription prior to a PCR amplification.