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제품 설명
Hifair™ V Multiplex One Step RT-qPCR Probe Kit (UDG Plus)
제품 번호
13650ES (1G)
제품 설명
Hifair™ V Multiplex One Step RT-qPCR Probe Kit (UDG Plus) is a multiplex quantitative PCR kit using RNA as the template. Reverse transcription and qPCR are performed in a single tube, simplifying the workflow and minimizing contamination risk.The kit uses a heat-stable Hifair™ V Reverse Transcriptase for efficient first-strand cDNA synthesis, and UNICON™ HotStart Taq DNA Polymerase for specific and robust amplification. It includes an optimized MP buffer with Mg²⁺, dNTPs, and additives that enhance specificity and multiplex amplification efficiency.
A dUTP/UDG system is incorporated to eliminate carryover contamination from previous PCR reactions, ensuring reliable results.
Components No. | Name | 13650ES50 (50 T) | 13650ES60 (100 T) | 13650ES80 (1,000 T) | 13650ES92 (10,000 T) |
13650-A | 2×HifairTM V MP Buffer | 750 μL | 1.5 mL | 15 mL | 150 mL |
13650-B | HifairTM V Enzyme Mix | 60 μL | 120 μL | 1.2 mL | 12 mL |
[Note]: 1) 2×HifairTM V MP Buffer is the abbreviation of HifairTM V Multiplex One Step RT-qPCR Probe Buffer, which includes dNTPs, dUTP, Mg2+, stabilizers, enhancers, and more.
2) HifairTM V Enzyme Mix mainly contains heat-resistant HifairTM V reverse transcriptase, UNICONTM HotStart Taq DNA polymeras and UDGase.
This product should be stored at -25~-15℃ for 18 months.
RT-qPCR Detection; Diagnostic pathogen detection (respiratory tract, intestinal tract, etc.); animal pathogen detection (non-swine fever, etc.); food testing (microorganisms, etc.)
1. Excellent amplification performance
Figure 1. Comparison of amplification performance of RT-qPCR kits from different brands
Amplification of gradient samples using 13650 and similar products from other suppliers in respiratory and HFMD panels showed clear S-shaped amplification curves. The Ct values of 13650 were comparable to or earlier than those of other kits, indicating superior performance.
2. Compatible with regular and fast programs
Figure 2. Test results of different reaction programs
Detection of ORF and N genes of SARS-CoV-2 pseudovirus using 13650ES under both regular and rapid programs showed no difference in amplification curve peak shape or Ct values in the 4-plex system.
3. Stability Test
Figure 3. Real-time stability testing(A) and Freeze-thaw stability(B)
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