One-step Universal Green RT-qPCR Kit

Quantitative PCR (qPCR), also known as Real-time PCR, is a highly versatile and precise technique for analyzing gene expression. According to the methodology, qPCR can be divided into two categories: dye-based methods and probe-based methods. Among these, dye-based methods are more universal, convenient, and cost-effective. Dye-based qPCR indirectly measures DNA amplification during each PCR cycle by monitoring the fluorescence emitted by dyes that bind specifically to double-stranded DNA (dsDNA). When the fluorescence signal detected at a certain time point significantly exceeds the background, the Ct value (also known as Cq value) can be determined. The obtained Ct values can be used to evaluate the relative abundance of the target gene or to calculate absolute quantities based on an appropriate standard curve.

The One-step Universal Green RT-qPCR Kit is convenient and efficient. It utilizes the real-time fluorescence signal of the dsDNA-binding dye SYBR Green I to monitor DNA amplification after each PCR cycle, enabling dye-based real-time quantitative analysis of target RNA sequences. The SYBR Green RT-qPCR Enzyme Mix in this kit contains antibody-mediated hot-start Taq DNA polymerase and a novel reverse transcriptase with high thermal stability. The recommended reverse transcription temperature is 55°C, but it can be adjusted between 50°C -55°C. The 2× SYBR Green RT-qPCR Reaction Buffer contains dNTPs, SYBR Green I, and all necessary buffer components. Additionally, the premix includes a unique inert reference dye compatible with various qPCR instruments, including those requiring high or low ROX reference signals. Furthermore, the premix employs a thermolabile UDG+dUTP anti-contamination system, ensuring the accuracy of qPCR amplification results and reducing false-positive results caused by aerosol contamination. The kit also contains a non-fluorescent visible tracking dye, facilitating the visualization of reaction setup without interfering with real-time detection.