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One-step Probe RT-qPCR Mixes

For reproducible and efficient first-strand cDNA synthesis and subsequent Real-Time PCR in a single tube.

Features

  • Detects low copies of RNA targets from a broad range of samples
  • Exhibits consistent amplification across a wide dynamic range
  • Eliminates non-specific amplification through precisely selected anti-Taq antibody
  • Has a high efficiency in multiplex reactions
  • Detects molecular targets accurately as fast as 40 minutes with two or three steps cycling profiles

Product Details

One-Step Probe RT-qPCR Mix is a convenient reaction mixture for fast and reliable quantitative Real-Time PCR using probes, including TaqMan ®, Scorpions ® and molecular beacon probes.

It was created for reproducible and efficient first-strand cDNA synthesis and subsequent Real-Time PCR in a single tube. It is the best choice for probe-based Real-Time PCR assays, including singleplex and multiplex gene expression studies.

Performance

Assay Specification
DNase contamination None detected
RNase contamination None detected

 

Principle

Using high-affinity antibodies for hot-start polymerase ensures higher specificity by reducing the formation of primer-dimer structures. It allows for a more comprehensive dynamic range by removing competition for reaction reagents. It also leads to higher sensitivity and reproducibility.


Precisely optimized buffer components ensure optimal reverse transcriptase and hot-start polymerase activity conditions. Additionally, RNase Inhibitor protects RNA from unspecific RNases.


The One-Step Probe RT-qPCR Mix provides fast, highly specific one-step Real-Time RT-PCR results, giving consistent results across all commonly used Real-Time PCR platforms.

Procedure

Quality Control

One-Step Probe RT-qPCR Mix is extensively tested for its performance in different Real-Time PCR assays. It is free of DNase and RNase contamination.

Applications

This is used for applications such as:

  • RT-qPCR
  • Gene expression analysis and genetic profiling
  • miRNA profiling and quantification
  • Mass screening and RNA viral pathogen detection
  • Characterization of genetically modified organisms (GMO)

 

Resources

Safety Data Sheets (1)
Certificates of Analysis (1)
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