INTRODUCTION
TopPURE® FLUID VIRAL DNA/RNA EXTRACTION KIT is based on silica column technology in accordance with ISO 9001 and ISO 13485 standards, which allows simultaneous collection of high-quality DNA/RNA. The kit uses a CL lysis buffer to allow efficient lysis of a variety of starting materials, nucleic acids are then purified through two times washes to remove impurities. The results of purified shrimp are ready to use for downstream applications such as PCR, Real-time PCR, SNP, Southern Blot, etc.
TopPURE® FLUID VIRAL DNA/RNA EXTRACTION KIT
HIGHLIGHTS
- Simple and effecitive procedure
- High quality and purity
- Exclusion of hazardous chemicals like Phenol and Chloroform, ensuring safety in medical applications.
- Convenient: Provide a complete all chemical without needing to add chemicals or materials outside.
- The kit includes Ethanol for mixing Wash Buffer 1 and Wash Buffer 2
SPECIFICATIONS
- Input sample types: Cultured cells, bacteria, suspension, cleanup from the surface, fluid smear (medical) including SARS-CoV-2
- Input sample volume: 200 µL
- Elution buffer: 50 µL DNA/RNA
- Time-saving: 30 minutes /10 samples
- High purity: A260/A280 = 1.7 – 2.2
- Storage: Buffers can be stored dry at room temperature. Proteinase K stored at 2-8oC.
- Expiration date: 12 months from manufacture
COMPONENTS
| Component | Storage |
| CL buffer | Room temperature |
| WB1 Buffer | |
| WB2 Buffer | |
| EB Buffer | |
| PBS Buffer | |
| Ethanol | |
| Silica column | |
| Tube 1.5 mL | |
| Proteinase K | 2-8oC |
DATA EXPERIMENT
Figure 1. Comparison of the extraction quality of ABT (HI-712 – red line) and supplier N (blue line) on an ASFV suspension sample. Real-time PCR was then conducted by using ABT qPCR ASFV Mix
Figure 2. The 10% suspension sample (swine tissue) confirmed for ASFV positive, then diluted 10 times with PBS Buffer. DNA was extracted using the HI-712 Kit. Each diluted concentration was purified 3 times for repeatability.
