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Maxima Probe qPCR Master Mixes


Ready-to-use qPCR master mixes optimized for probe chemistry using standard cycling protocols
  
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Thermo Scientific Maxima Probe qPCR Master Mixes are ready-to-use solutions optimized for quantitative real-time PCR. The master mixes include Maxima Hot Start Taq DNA Polymerase and dNTPs in an optimized PCR buffer. Only template and primers need to be added.

Maxima Hot Start Taq DNA Polymerase in combination with an optimized buffer ensures PCR specificity and sensitivity. dUTP is included in the mix for optional carry-over contamination control using uracil DNA glycosylase (UDG) (see Reference 1). The use of Maxima Probe qPCR Master Mixes in real-time PCR ensures reproducible, sensitive and specific quantification of genomic, plasmid, viral, and cDNA templates.

Maxima Probe qPCR Master Mixes are compatible with most real-time thermal cyclers.

Highlights

  • SpecificityMaxima Hot Start Taq DNA Polymerase and the optimized buffer eliminate non-specific amplification and formation of primer dimers
  • Sensitivity – detects low copy number targets
  • Wide linear range – accurate quantification across 9 orders of magnitude
  • Reproducibility and convenience – ready-to-use 2X master mix

Applications

  • Gene expression
  • siRNA validation
  • Genotyping
  • Pathogen detection

Includes

All Maxima Probe qPCR Master Mixes include Maxima Hot Start Taq DNA Polymerase and dNTPs (also dUTP) in an optimized PCR buffer. Supplied with nuclease-free water.

  • Maxima Probe/ROX qPCR Master Mix (2X) is supplemented with ROX passive reference dye.
  • Maxima Probe qPCR Master Mix, ROX Solution provided (2X), comes with a separate ROX vial.
  
Storage Condition-20 C
HazardousNo
Storage notesNote that ROX dye is light sensitive; exposure should be minimized.
Amplification data for human PPP1CA gene

Highly sensitive two step qRT-PCR

Amplification data for human PPP1CA gene

Amplification of human PPP1CA gene was performed on serial 10-fold dilutions of Jurkat cell total RNA (from 1 ng to 1 pg). First strand cDNA was generated with the RevertAid First Strand cDNA Synthesis Kit. cDNA was amplified with the Maxima Probe/ROX qPCR Master Mix (2X) using the TaqMan® assay specific for PPP1CA. Reactions were performed on an ABI PRISM 7000 instrument. 1 pg of total RNA was successfully detected. NTC is the non-template control.


Amplification data for human PGK1 gene

Precise and reproducible results

Amplification data for human PGK1 gene

Amplification of human PGK1 gene was performed on serial 2-fold dilutions of human genomic DNA (from 0.5 µg to 1 ng) in a replicate reactions of 25 µL. Reactions were performed on an ABI PRISM® 7000 instrument. NTC is the non-template control.


References

  1. M. C. Longo et al., Use of uracil DNA glycosylase to control carry-over contamination in Polymerase Chain Reactions. Gene. 93(1), 125-128 (1 September 1990).