page_banner

Products

GSBIO Nucleic Acid Extraction Magnetic Beads

Short Description:

Product Features

1. Applicable to a wide range of samples, able to isolate viral DNA/RNA, genomic DNA, PCR fragments, plasmid DNA, etc.

2. High batch-to-batch stability.

3. Adaptable to automation (slow settling speed, fast magnetic response, high adsorption in short time).

4. Adaptable to different customer requirements (different particle sizes and bead concentrations are customizable).

5. Outstanding performance in viral DNA extraction.


Product Detail

Product Tags

GSBIO Silicon Hydroxyl Magnetic Bead has a superparamagnetic core and a silica shell with a lot of silane alcohol groups for efficient capture of nucleic acids. Traditional methods for isolating nucleic acids (DNA or RNA) include centrifugation or phenol-chloroform extraction. Magnetic separation using silicon hydroxyl magnetic beads is ideal for extracting nucleic acids, which can be rapidly and safely isolated from biological samples by mixing silicon hydroxyl magnetic beads with chaotropic salts.

Parameters

GSBIO Silicon Hydroxyl Magnetic Beads (- Si-OH)
Particle size: 500nm
Concentration: 12.5mg/ml, 50mg/ml
Packing specifications: 5ml, 10ml, 20ml
Dispersibility: Monodisperse

Applications

⚪DNA and RNA Extraction: Silicon hydroxyl magnetic beads can be used to efficiently, rapidly and safely extract and purify DNA and RNA from a wide variety of biological samples such as blood, cells, viruses and so on.

⚪PCR product purification: Silicon hydroxyl magnetic beads can be used to purify and enrich PCR reaction products, remove impurities and by-products, thus improving the specificity and sensitivity of the PCR reaction.

⚪NGS pre-treatment: Silicon hydroxyl magnetic beads can be used for nucleic acid extraction and purification before gene sequencing to improve the quality and accuracy of sequencing results.

⚪RNA methylation sequencing: Silico hydroxyl magnetic beads can be used to enrich and purify methylated RNA for RNA methylation sequencing.


  • Previous:
  • Next:

  • Write your message here and send it to us