PCR principle: The essence of PCR technology is nucleic acid amplification in vitro, heat to uncoil double stranded DNA, hybridize primer with template DNA at annealing temperature, extend primer in the presence of Taq DNA polymerase, dNTPs, Mg2+ and suitable pH buffer, repeat the process of "denaturation ? annealing ? primer extension" to 25 ~ 40 cycles. Exponentially expand the nucleic acid copy number in the sample to be tested. 1\Temperature Accuracy: ±0.2 degree 2\Temperature uniformity: +0.25 degree 3\Temperature Input Range: At room temperatureto 99 degree 4\Rate of temperature change: heating rate >6?/s;cooling rate >4?/s 5\Light life ? 100,000 hours 6\Fluorescence channel: 2 channels 7\Samples per instrument: 2×8 Wells 8\Reaction volume range: 10-100ul,0.2ml 9\Hardware parameters: With touch screen,the experimental process can be viewed in real With touch screen,the experimental process can be viewed in realtime;The device supports connecting to the cloud service platfom,a time;The device supports connecting to the cloud service platfom,and can realize functions such as automatic data transmission and nd can realize functions such as automatic datatransmission and remote consulting. 10\Communication module: USB,Wifi. The device can be connected with a code scanning gun and input sample information 11\Physical parameters: Small size,easy to carry;External 373×330×145mm(L×W×H) 12\Weight: 4kg

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