Nucleic acid fragment screening kit

Extremely high repeatability
NGS is widely used in the discovery, prenatal diagnosis, and personalized medication of diseases such as tumors. Different brands of sequencers can effectively read DNA fragments of varying sizes. The size of DNA fragments directly affects the validity of sequencing data. SPRI's magnetic bead technology not only ensures high reproducibility of experimental results, but also allows operators to freely choose the range of fragments that need to be screened.
1. SPRI magnetic bead principle, no need for cutting glue, easy to operate
2. The range of nucleic acid size selection can be freely selected
3. Both manual and automated workstations can be used
4. Automated workstations can process 96 samples simultaneously
5. Next Generation Sequencing (NGS) Sample Library Establishment Designated Reagent Kit

DNA Size Selection is an essential experimental process in the NGS sample library construction process. Its purpose is to screen the interrupted DNA into specific interval ranges, such as 300-600bp or 200-400bp. Only data with specific fragment lengths can ensure the validity of sequencing results. The SPRIselect kit can perform Left side Size Selection, Right side Size Selection, and Double size Selection to meet the needs of different length ranges of nucleic acids.

Left-side Size selction Remove the small segment on the left
Right-side Size Selection Remove the large segment on the right side
Double Size Selection Simultaneously removing the small segment on the left and the large segment on the right, Obtain the intermediate target fragment	product Composition of reagent kit Item number SPRIselect 5 mL Reagent Agencourt SPRIselect Reagent B23317 SPRIselect 60 mL Reagent Agencourt SPRIselect Reagent B23318 SPRIselect 450 mL Reagent Agencourt SPRIselect Reagent B23319

*The content and products mentioned in this article are only used for scientific research and industry, and are not intended for clinical diagnosis.