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Guide
At present, there are many brands of hot-start Taq enzyme sold in the domestic market, but there are not many really high-quality hot-start Taq enzymes, in the face of so many hot-start Taq enzyme products, how should we choose?
First, warm-start Taq enzymes with high amplification efficiency are selected
After the well-tolerated Taq enzyme reaction system is optimized, the amplification efficiency is more than 95%, and the amplification can be obtained satisfactorily even when the content of the target gene is low, and it is not easy to be poisoned when the amount of template is high, and the exponential amplification period is longer
Second, choose a hot-start Taq enzyme with strong enzymatic power
The enzymatic motility of taq enzymes is related
Generally speaking, DNA polymerase amplification efficiency is high, the sensitivity is high, but there are also inconsistencies
The amplification sensitivity of Taq enzyme is detected, and the common detection method is to dilute the plasmid fragment of the target gene by 10x or 5x gradient, perform PCR detection at a few lower dilutions, and select the hot-start Taq enzyme
It can be seen that researchers need to choose according to their own experimental requirements and funding, and it is best to do a gradient dilution amplification experiment to detect the amplification efficiency and sensitivity
CieloTM real-time PCR system
Harness of the power of qPCR
▌ 12 columns of temperature gradient settings: multi-temperature gradient settings, quickly optimize conditions, determine the appropriate annealing temperature
▌ Good S-type amplification curve
▌ The melting curve is single-peaked, without miscellaneous peaks
In addition, Cielo's™ real-time PCR system combines high-quality Peltier temperature modules with optical inspection systems based on fiber optic transmission to provide highly accurate, sensitive and reliable results
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