50 ml, 2x real-time PCR mix, contains dNTPs, Sso7d fusion polymerase, MgCl2, EvaGreen dye, stabilizers, for 5,000 x 20 µl reactions
Bio-Rad introduces the SsoFast™ EvaGreen® supermix, a member of our next generation of real-time PCR supermixes using our patented Sso7d fusion protein technology, delivering a reagent that provides effective performance in a wide range of qPCR applications. The dsDNA-binding protein, Sso7d, stabilizes the polymerase-template complex, increases processivity, and provides greater speed and reduced reaction times compared to conventional DNA polymerases, without affecting PCR sensitivity, efficiency, or reproducibility.
Key Features and Benefits
Fast qPCR results and high performance — the Sso7d fusion polymerase and optimized buffer deliver fast reaction times via instant polymerase activation and rapid polymerization kinetics to generate exceptional qPCR results in less than 30 min
Minimal inhibition of PCR — the polymerase's increased resistance to PCR inhibitors ensures maximum efficiency, sensitivity, and reproducibility, and provides increased fluorescence compared to SYBR® Green
Single copy detection — data illustrate high sensitivity with amplification and detection from a single copy of target gene
Robust discrimination and reproducibility — efficient discrimination and reliable quantification can be obtained from 1.33-fold serial dilutions of input template
Applications and Uses
Dye-based qPCR detection
PCR and real-time PCR analysis
Nucleic acid amplification and expression profiling
Gene expression analysis
Genotyping studies
Genomics-related applications
50 ml, 2x real-time PCR mix, contains dNTPs, Sso7d fusion polymerase, MgCl2, EvaGreen dye, stabilizers, for 5,000 x 20 µl reactions
Bio-Rad introduces the SsoFast™ EvaGreen® supermix, a member of our next generation of real-time PCR supermixes using our patented Sso7d fusion protein technology, delivering a reagent that provides effective performance in a wide range of qPCR applications. The dsDNA-binding protein, Sso7d, stabilizes the polymerase-template complex, increases processivity, and provides greater speed and reduced reaction times compared to conventional DNA polymerases, without affecting PCR sensitivity, efficiency, or reproducibility.
Key Features and Benefits
- Fast qPCR results and high performance — the Sso7d fusion polymerase and optimized buffer deliver fast reaction times via instant polymerase activation and rapid polymerization kinetics to generate exceptional qPCR results in less than 30 min
- Minimal inhibition of PCR — the polymerase's increased resistance to PCR inhibitors ensures maximum efficiency, sensitivity, and reproducibility, and provides increased fluorescence compared to SYBR® Green
- Single copy detection — data illustrate high sensitivity with amplification and detection from a single copy of target gene
- Robust discrimination and reproducibility — efficient discrimination and reliable quantification can be obtained from 1.33-fold serial dilutions of input template
Applications and Uses
- Dye-based qPCR detection
- PCR and real-time PCR analysis
- Nucleic acid amplification and expression profiling
- Gene expression analysis
- Genotyping studies
- Genomics-related applications
