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PCR amplification reagent
The PCR amplification reaction uses the patented technology STH-PAS (Single Tag Hybridization-Printed Array Strip),
through a pair of 5'-end specially modified specific primers, with PCR reaction solution, hot-start Taq enzyme and other components for specificity PCR amplification.
Detection device
Followed by reconstitution and release of the PCR amplification product and blue latex microspheres in the detection device,
and the released amplification product hybridizes with the probe on the membrane strip and fixes it. Make a qualitative interpretation by the presence or absence of blue bands.
Advantage:
- Disposable anti-pollution detection device with the principle of physical isolation, does not need to open the cover to process PCR amplification products, which can effectively avoid false positives caused by aerosol diffusion of PCR amplification products.
- Adopts the dUTP-UNG enzyme anti-pollution system,eliminating the existing U-DNA pollutants in the reaction system or the environment.
- Equipped with internal standard system, negative control and positive control,participates in the parallel extraction and detection of sample nucleic acid.