Product Description
Hifair™ Lyo-Ready I Multiplex One Step RT-qPCR Kit(UDG plus) is an optimized reagent for fast and sensitive amplification and quantitation of RNA targets with probe-based assays. In the process of the experiment, reverse transcription and quantitative PCR were carried out in the same tube, which simplified the experimental operation and reduced the risk of contamination.The unique Buffer and enzyme design ensures that it can be used in the preparation and product design of one-step RT-qPCR lyophilized reaction systems. The kit mainly contains Hifair™ V Reverse Transcriptase, Hieff UniconTM HotStart Taq DNA Polymerase and optimized lyophilizable buffer,etc. In addition, the factors that can effectively inhibit the non-specific PCR amplification and improve the amplification efficiency of multiple qPCR reactions are added, which can ensure the amplification efficiency and carry out up to multiple amplification reaction.
This kit is fitted with lyoprotectant that can be used for lyophilization.
Features
Applications
Specifications
Components
Shipping and Storage
This product should be stored at -25~-15℃ for one years. It should avoid repeated freezing and thawing.
Figures
1. Freeze-dried products in various forms
Figure 1. Freeze-dried product form In situ freeze-drying and freeze-dried microspheres. The freeze-dried morphology was good after freeze-drying, there was no collapse on the in situ freeze-dried surface, and there was no gap in the tube; the freeze-dried microspheres were plump and smooth in shape and uniform in size. 2. Consistent performance
Figure 2. Consistent performance between Liquid reagent and lyophilized Microspheres 3. Stability test
Figure 3. Freeze-dried microspheres accelerate stability test After being freeze-dried into freeze-dried microspheres using Yeasen's RNA lyophilizable reagent (Catt#1 6645 ES), placed under different conditions (accelerated at 50°C for 33 days), and 10 4 , and 10 3 copies/mL of HPIV pseudovirus templates were amplified simultaneously. The results showed that there was no significant change in the Ct value, fluorescence value, spherical shape, etc. of the freeze-dried microspheres before and after thermal acceleration, and the freeze-dried product had good stability. 4. Mutiplex PCR Amplification of pathogens
Figure 4. Multiplex amplification of pathogens ( HPIVs Template concentration E6/5/4/3/2/1 )
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