Nucleic acid detection is essentially realized by using the PCR reaction (polymerase chain reaction) we learned in high school biology books. The PCR reaction utilizes the double-strand replication principle of DNA to amplify a large number of target genes in vitro. The nucleic acid amplification stage requires the use of a PCR instrument, which can automatically "denature-anneal-extend" the submitted liquid to amplify the amount of nucleic acid. It seems very simple, but in fact it is very time-consuming from nucleic acid collection to results.
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