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RealQ Plus Master Mix for Probe

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RealQ Plus Master Mix for Probe enables real-time-based DNA amplification with high specificity and efficiency. Real-time PCR is a sensitive and reliable method for ge





















FEATURES

  • Promotes probe-based real-time PCR based detection
  • Enables multiplexing
  • Very high specificity
  • High stability and efficiency
  • Reliable quantification
  • Reaction set-up at room temperature
  • Premixed all-in-one 2x solution


DESCRIPTION

RealQ Plus 2x Master Mix for Probe is composed of TEMPase Hot Start DNA Polymerase, dNTPs, dye and an optimised buffer system. Furthermore, this master mix is available with high, low or without ROXTM ensuring optimal performance on most of the commonly used real-time PCR instruments. Just add DNA template, primers and probe.

The RealQ Plus 2x Master Mix for probe is optimised to TaqMan probes, but is also suitable with other probe chemistries such as Molecular Beacon and Scorpion. 

Most probe-based detection methods take advantage of fluorescent resonance energy transfer (FRET) by quenching the signal of a fluorescent reporter in the absence of the desired target. During elongation, the quenching molecule is separated from the fluorescent reporter and a signal is emitted and monitored. Probe-based detection is significantly more specific since signal is only detected when the correct target is amplified.

 

ROX SELECTION GUIDE

Use this guide to select the correct level of ROX™ reference dye for your real-time PCR application.

 

 

































HIGH EFFICIENCY AND PRECISION
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Amplification plot of a 4-fold dilution series for a Pthr target (75 bp) amplified from human gDNA, starting with 80 ng down to 80 pg of gDNA, using RealQ Plus 2x Master Mix for Probe, High ROX™. Samples were made in triplicates. The results depicted here, show high precision and efficiencies close to 100 %.

REPRODUCIBILITY
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80 replicates of RealQ Plus 2x Master Mix Green, High ROX™ and 20 ng gDNA, show a standard deviation of only 0.084.


STABILITY AT ROOM TEMPERATURE

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Two plates were pre-assembled for qPCR reaction and incubated in darkness at room temperature for 48 and 72 hours. The results show high stability and complete inactivation of the TEMPase before hot start. It allows the scientist to set up the reaction and run the plate several hours later, when convenient.



PRODUCT INFO

RealQ Plus Master Mix for Probe

For Probe without ROX 

For Probe with low ROX 

For Probe with high ROX 

 


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