• StarPure DNA Fragment Selection Kit-V2
  • StarPure DNA Fragment Selection Kit-V2

StarPure DNA Fragment Selection Kit-V2

No.FS-B5004/FS-B5005/FS-B5006
This kit utilizes uniquely engineered nanomagnetic beads and a specialized buffer system for nucleic acid purification. It can also be used to isolate and purify nucleic acid fragments within a target size range from mixed nucleic acid samples by varying the loading ratio. The entire process is safe and convenient, with high recovery rates and reliable quality. The magnetic bead separation system is particularly well-suited for automated extraction in high-throughput workstations.
Item No./Specifications/Price:
FS-B5004/5 mL/¥500.00
FS-B5005/60 mL/¥3000.00
FS-B5006/450mL/¥19125.00
  • StarPure DNA Fragment Selection Kit-V2

Product Description

StarPure DNA size Selection Kit-V2
StarPure DNA Fragment Selection Kit-V2



Product Advantages
  • Nanomagnetic bead-based nucleic acid fragment purification and sorting technology can sort out nucleic acids within a specific size range;
  • Suitable for manual extraction and automated workstation use;
  • Purified or sorted products can be used for PCR, next-generation sequencing, etc.
  • This product does not require organic reagents such as phenol/chloroform, and the operation process is safe and fast.

    Product Application

    It can be used for nucleic acid purification, and can also separate and purify nucleic acid fragments within the target size range from mixed nucleic acid samples through different loading ratios.

    Product components


    Product Performance

    1. Excellent fragment sorting effect and recovery efficiency


    Figure 1. A 3-ng sample of enzymatically sheared human DNA was used for library construction using the KAPA Hyperprep library preparation kit. After amplification, 300 ng of the library product was fractionated using 0.5X/0.7X, 0.6X/0.8X, and 0.7X/0.9X filters, respectively. After fragment sorting, fragment size distribution was analyzed using the Bioanalyzer@ 2100 high-sensitivity kit.
    Figure 2. Using the same library sample, fragments were sorted at 0.6x/0.8x using Qihengxing, 0.7x/0.9x using Supplier B, and 0.7x/0.9x using Supplier K, respectively. After fragment sorting, fragment size distribution was analyzed using the Bioanalyzer@ 2100 High Sensitivity Kit.
    Related Product Links
    NGS related products (Qubit series/DNA fragment selection & purification/library quantification)

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