High performing probe-based qPCR Mix for AT-rich, regular and GC-rich templates
Description
HOT FIREPol® Probe Universal qPCR Mix is optimized for real-time quantitative PCR assays and contains all the components necessary to perform singleplex or duplex qPCR, with the exception of template, primers, and probes. Proprietary reaction buffer that enables efficient amplification of regular and GC-rich targets.
HOT FIREPol® Probe Universal qPCR Mix is optimized for DNA/LNA hydrolysis probes based on the 5′ flap endonuclease activity.
The Mix contains internal passive reference dye that is compatible with most qPCR cyclers including high ROX or low ROX reference signal requiring platforms.
The Mix contains dUTPs to prevent cross-contamination with UNG treatment.
Mix Components
HOT FIREPol® DNA Polymerase: chemically modified FIREPol® DNA Polymerase enabling hot-start
5x Probe Universal qPCR buffer with 15 mM MgCl2: 1x PCR solution – 3 mM MgCl2
dNTPs including dUTP: Mix allows UNG treatment to prevent carryover contamination from previous runs.
IMPORTANT: UNG is not included in the HOT FIREPol® Probe Universal qPCR Mix
Reference dye based on ROX: For multiplex application – if ROX dye is used as one of the fluorophores, the internal reference might interfere with the signal.
In separate vial
100% DMSO is included in the kit in a separate vial. DMSO is recommended as a PCR additive for templates with high GC content. In some cases, DMSO is also required to relax secondary structures.
Properties
Concentration: 5x
Hot-start: yes, initial activation in 10 min
Detection type: Probe-based
Reference dye: reference dye based on ROX
Compatible real-time instruments: Most qPCR platforms.
Applications
- DNA/LNA hydrolysis probe-based assays
- Detection and quantification of DNA and cDNA targets
- Profiling gene expression
- Microbial detection
- Viral load determination
ABT Equipment Co., Ltd is proud to be the official distributor of Meridian Bioscience – Bioline. If you have any questions or need further assistance, please contact: