Overview:
Based on real-time fluorescence PCR technology, primers and fluorescent probes are designed for detecting target specific gene fragments, and the required reagent components for the reaction are optimized. The amplification reaction can be carried out by adding the nucleic acid of the test sample. During the amplification process, the fluorescent probe binds to the target gene fragment and can be decomposed by Tag enzyme to generate a fluorescent signal. At this time, the fluorescence quantitative PCR instrument can recognize the fluorescent signal and draw the corresponding real-time amplification curve based on its strength changes, thereby determining whether the target gene has been detected.
Features:
Quick extraction: One step nucleic acid extraction, fast and efficient, with high nucleic acid extraction efficiency;
Easy to operate: Provide a pre mixed PCR reaction system for direct sample testing without the need for self preparation;
Strong specificity: using highly specific primers and probes to ensure experimental accuracy;
High sensitivity; Using efficient amplification enzymes, the detection sensitivity can reach as low as 1-10 copy/test.
