DNA SizeSelector-I

Price range: $125.00 through $675.00

Easy-to-use kit solution that effectively eliminates adapter contamination, ensuring high-purity DNA recovery.

 

Category: SKU: Z-6001

Available Options:

Description

Product Details

The DNA SizeSelector-I is an easy-to-use solution that effectively eliminates adapter contamination, ensuring high-purity DNA recovery. By removing unwanted adapters from the reaction, DNA SizeSelector-I streamlines NGS library preparation and optimizes sample quality for high-sensitivity downstream sequencing.

Note: Use twice to remove all adaptors in the reaction for DNA clean up.

 

Key Features

  • Optimized DNA recovery in 200~800bp range
  • Complete removal of adaptors
  • Compatible with all NGS platforms (e.g.s Illumina, Pacific Bio, Roche’s 454)
  • Simplified procedure compared to Ampure™: one step size selection
  • No further clean-up steps necessary
  • Compatible with manual and automated processes
  • More efficient and cost-effective

Sizes:

  • 5 preps
  • 50 preps
  • 250 preps

Packaging:

  • 645 reactions per box

Storage:

  • Store at 4°C upon arrival, DO NOT FREEZE

Stability:

  • 12 months if stored as specified

 

Disclaimer: For research use only. Not for use in diagnostic procedures.

 

Protocols
Protocol-ALINE DNA SizeSelector I - v15.1 _1_

 

Published Journal References:

  1. R. Darwiche, & K. Struhl, Proc. Natl. Acad. Sci. U.S.A. 117 (46) 28925-28929;
    Pheno-RNA, a method to associate genes with a specific phenotype, identifies genes linked to cellular transformation.
    https://www.pnas.org/doi/10.1073/pnas.2014165117
  2. Tan et al., Molecular Biology of the Cell, 2014;
    A microscopy-based screen employing multiplex genome sequencing identifies cargo-specific requirements for dynein velocity.
    http://www.ncbi.nlm.nih.gov/pubmed/24403603/
  3.  KH Wong et al., Current Protocols in Molecular Biology, 2013, 101:7.11 1-7.11.11
    Multiplex Illumina Sequencing Using DNA Barcoding.
    http://www.ncbi.nlm.nih.gov/pubmed/23288465
  4. Reinholdt et al., Mamm Genome, 2011, 22:685-691 Molecular Characterization of the Translocation Breakpoints in the Down Syndrome Mouse Model, Ts65Dn.
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505986