| Cat# | Kit-054 |
| Description | This kit is designed for high-quality DNA library construction on Illumina sequencing platforms. It employs an engineered transposase to fragment DNA, converting DNA fragmentation, end repair, and adapter ligation into a single enzymatic reaction. This streamlined workflow significantly reduces required input DNA and shortens library preparation time. As an upgraded version of earlier transposase-based kits, this version further optimizes the library construction process, delivering higher-quality libraries while maintaining low background nucleic acid interference. It is suitable for applications requiring rapid, efficient, and reproducible Illumina-compatible library preparation. |
| Storage | -30 °C to -15 °C |
| Applications | Whole-genome sequencing; library construction from single-cell amplified products; mNGS testing. |
| Product Overview | Unified workflow: Simpler and more time-efficient. Improved data quality: Reduced GC bias, lower false positives, and superior pathogen detection. Innovative adapter-dimer-free technology: Enables library construction with low input without generating adapter dimers. |
| Package | 24 rxns TruePrp Tagmet Enzyme Mix P50: 96 μL 5x TruePrp Tagment Buffer L: 96 μL Universal Neutalization Buffer: 96 μL Amplification Mix: 384 μL Control DNA (Mouse Genomic DNA, 50 ng/μL): 10 μL |
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