Cost-effective dye-based qPCR Mix without passive reference dye ROX.
High sensitivity and specificity.
Excellent efficiency.
Reaction set-up and shipment without dry ice.
Cost-effective solution for a wide range of applications.
Description
Dye-based real-time quantitative PCR (qPCR) uses DNA binding dye to evaluate the DNA amplification process during PCR. In this mix EvaGreen® double-stranded DNA binding dye is used instead of the more widely used SYBR Green I that has similar fluorescence spectra. Compared to SYBR Green I dye EvaGreen® dye shows a higher fluorescence level, high sensitivity for detecting low template concentrations, and high stability at room temperature.
HOT FIREPol® EvaGreen® qPCR Mix Plus (no ROX) is an optimized ready-to-use solution for dye-based real-time quantitative PCR assays on cyclers that do not require passive reference dye.
Properties
Concentration: 5x
Hot-start: yes, initial activation in 12-15 min
Detection type: dye-based, includes EvaGreen® intercalating dye
Reference dye: none
Compatible real-time instruments: Cyclers that do not require ROX reference dye.
Mix Components
HOT FIREPol® DNA polymerase: chemically modified FIREPol® DNA Polymerase enabling hot-start
5x EvaGreen® qPCR buffer with 12. 5 mM MgCl2: 1x PCR solution – 2.5 mM MgCl2
dNTPs: dATP, dCTP, dGTP and dTTP
EvaGreen® dye
Some applications of this product may require a license which is not provided by the purchase of this product.