Remark:
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.
±0.2℃ |
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Temperature uniformity |
+0.25℃ |
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Temperature Input Range |
At room temperatureto 99℃ |
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Rate of temperature change |
heating rate >6℃/s;cooling rate >4℃/s |
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Light life |
≥ 100,000 hours |
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Fluorescence channel |
4 channels |
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Samples per instrument |
2×8 Wells |
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Reaction volume range |
10-100ul,0.2ml |
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Hardware parameters |
With touch
screen,the experimental process can be viewed in real With touch screen,the
experimental process can be viewed in real |
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Communication module |
USB,Wifi |
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Physical parameters |
Small size,easy to carry;External |
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373×330×145mm(L×W×H) |
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Weight |
4kg |