Hieff UNICON™ ColorGPS qPCR Master Mix (High Rox) is a pre-solution for 2×real-time quantitative PCR amplification, featuring high fluorescence intensity, high sensitivity and specificity, and high amplification yield. The core component, Hieff UNICON™ Taq DNA Polymerase, is hot-started by antibody method, which can effectively inhibit non-specific amplification caused by primer annealing during sample preparation. At the same time, the formula adds factors to enhance the amplification efficiency of the PCR reaction and facilitators to equalize the amplification of genes with different GC contents (30~70%), so that the quantitative PCR can obtain a good linear relationship in a wide range of quantitative regions. The product utilizes the mixed color change reaction of different dyes to monitor the pipetting operation, which effectively reduces the occurrence of pipetting errors. Features Pipetting Tracking: Reduce the Risk of Missed/Addition Errors Excellent Amplification: Good linearity across a wide linear range High Precision: Can accurately distinguish templates with a 2-fold concentration difference Good Repeatability: Small inter-well variability in replicate wells, resulting in better repeatability Stable and Reliable: The reaction system can be stored at room temperature for 24 hours, and the product remains unaffected after 20 freeze-thaw cycles Applications Gene Expression Difference Analysis Absolute Quantitative Analysis Specifications Concentration 2 ×(qPCR Mix) Detection method Dye method PCR method qPCR Polymerase Taq DNA Polymerase Type of sample DNA Application equipment Biosystems 5700, 7000, 7300, 7700, 7900, 7900HT, 7900HT Fast, StepOne, StepOnePlus and other fluorescence quantitative PCR instruments that require the addition of high concentrations of ROX Reference Dye Product Type Premix for real-time fluorescence quantitative PCR Apply to (application) Gene Expression Components Components No. Name 11190ES03 11190ES08 11190ES60 11190-A Hieff UNICON™ ColorGPS qPCR Master Mix (High Rox) 1 mL 5×1 mL 100×1 mL 11190-B 10×Dilution Buffer 1 mL 1 mL 20×1 mL Figures Pipetting Tracking Reduces the Risk of Missed or Incorrect Additions Pipetting tracking provides clear visualization of the workflow. Samples were added according to the product instructions, with templates containing different colored dyes each added at a final volume of 2 μL. The results show that Yeasen’s new pipetting tracking feature clearly displays the sample addition progress. [Note]: 11190ES is the High ROX version of 11188ES. Figure 1. Reliable results can be obtained within the dynamic range. Using 2 µL of plasmid templates with a gradient of 10^1-10^7, the related genes were amplified. Hieff UNICON™ ColorGPS master mix can effectively detect a template amount range of 7 orders of magnitude, achieving good linearity within a broad linear range. Figure 2. Can accurately distinguish template concentration differences of 2-fold. Using 2 µL of plasmid diluted in a 2-fold gradient as the template, the related genes were amplified. Hieff UNICON™ ColorGPS master mix can accurately resolve template concentration differences. Figure 3. Small inter-well variability is observed, showing better repeatability. Using dozens of copies of plasmid as the template, amplification was performed with different fluorescent quantitative reagents according to the procedures specified in their respective instruction manuals. The SD values indicate that, compared to other reverse transcription reagents, the new product has smaller differences between replicate wells and better repeatability. Figure 4. More flexible, suitable for standard or rapid procedures. In the standard procedure, the denaturation time and extension time are set to 10 seconds and 30 seconds, respectively, while in the rapid procedure, the denaturation time and extension time are set to 3 seconds and 10 seconds, respectively, to detect the Ct values corresponding to 10 target genes. The results show that the Ct values obtained with the new product in both standard and rapid procedures have a strong correlation, and the new product can achieve good results using the rapid procedure. Figure 5. After the reaction system is prepared, it can remain stable at room temperature for 24 hours. Using different genes from mouse, human 293 cells, and Arabidopsis thaliana as targets, after preparing the reaction system, it was placed in the dark at different temperatures for 24 hours before detection. Compared to immediate processing, the detection difference for different genes does not exceed 0.5 Ct, indicating that stable results can also be obtained with long-duration operations. Try it for free! Get a free sample of ColorGPS qPCR Master Mix and validate its performance in your own lab.👉 [Request Sample Now]
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