• 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 uses nanomagnetic beads with unique separation effects and a special buffer system. 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. The whole process is safe and convenient. The recovery rate is high and the quality is stable and reliable. The magnetic bead separation system is particularly suitable for automated extraction in high-throughput workstations.
Item No./Specification/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
  • The nucleic acid fragment purification and sorting technology based on nanomagnetic beads 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.

    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 composition


    Product Performance

    1. Excellent fragment sorting effect and recovery efficiency


    Figure 1. Human DNA cut with enzymes was used as the sample (3 ng) and the library was constructed using the kapa hyperprep library preparation kit. 300 ng of the amplified library products were taken and fragmented using 0.5X/0.7x, 0.6X/0.8x, and 0.7X/0.9X, respectively. After fragment selection, the Bioanalyzer@ 2100 high-sensitivity kit was used to analyze the fragment size distribution.
    Figure 2. The same library sample was used for fragment sorting using Qihengxing, Supplier B, and Supplier K at 0.6x/0.8x and 0.7x/0.9x, respectively. After fragment sorting, the 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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