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SYBR® GreenER™ qPCR SuperMixes Universal incorporate the latest high-performance technology to provide the most reliable gene expression data on a variety of platforms, including ABI 7500, Corbett Rotor-Gene™, MJ Chromo4™ and Opticon™, and Stratagene instruments. The SYBR® GreenER™ system is specially formulated to offer the best sensitivity, specificity, and reproducibility with: • A novel dsDNA-binding dye - exhibits a brighter signal for increased sensitivity and less PCR inhibition than original SYBR® Green I, while using the same instrument filters and settings • An optimized buffer system - improves sensitivity and provides excellent long-term stability • Uracil DNA glycosylase - reduces carryover contamination in qPCR
Novel Formulation Provides More Reliable Data The SYBR® GreenER™ qPCR SuperMix kits include a new dsDNA-binding dye that produces a brighter signal and significantly less PCR inhibition, for improved qPCR performance over a broad dynamic range.
Consistent Specificity and Low-Copy Detection The SYBR® GreenER™ qPCR reagent system minimizes the formation of nonspecific products, including primer-dimers, for greater accuracy across a wide range of targets. The reliability of the SYBR® GreenER™ qPCR reagent system also translates to greater sensitivity. With SYBR® GreenER™ qPCR SuperMix, you can consistently detect fewer than 10 copies of a target in genomic DNA.
Eight cDNA targets and eight genomic DNA targets were amplified from 1 ng of cDNA and 6 pg of gDNA, respectively, on the ABI PRISM® 7900HT Sequence Detection System using the SYBR® GreenER™ qPCR SuperMix for ABI PRISM® instruments. For all 16 targets, detection was positive in the presence of template but negative for all no-template controls.
For Research Use Only. Not for use in diagnostics procedures.
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