Products & ReviewLife Sciences

SureSelect XT HS2 DNA Reagent Kit

Agilent TechnologiesAvailable: Worldwide

The SureSelect XT HS2 DNA Reagent Kit is Agilent’s most cutting-edge library prep and target enrichment solution for Illumina sequencing

Agilent Technologies

The supplier does not provide quotations for this product through SelectScience. You can search for similar products in our  Product Directory.

Average Rating 4.8

|2Scientists have reviewed this product

Ease of Use
After Sales Service
Value for Money
Write your own review

Great ease of use and automation great robustness

 

Average Rating 4.7

Application Area:

Genome sequencing

Highly sensitive and enable detection of single-nucleotide, DNA/RNA structural and copy number variants, fusions, mutations and insertions and deletions

Review Date: 1 Dec 2023 | Agilent Technologies

Good product for strand-specific RNA library enrichment, for low input samples.

 

Average Rating 5.0

Application Area:

RNA Seq library preparation

Good product for strand-specific RNA library enrichment. Worked well for low input samples.

Review Date: 18 Nov 2021 | Agilent Technologies

The SureSelect XT HS2 DNA Reagent Kit is Agilent’s most cutting-edge library prep and target enrichment solution for Illumina sequencing. It provides a streamlined workflow, excellent performance and comprehensive features that can satisfy most of your NGS library prep needs. The modular configuration enables an easy and parallel workflow for RNA and DNA sequencing using SureSelect XT HS2 chemistry.

This high sensitivity kit is equipped with molecular barcodes to detect low frequency alleles. A total of 384 unique dual indexing allows you to multiplex hundreds of samples and not worry about index hopping. Its ultimate flexibility enables you to choose the workflow that best fits your needs.

Features:

  • Generate high-quality libraries with as little as 10 ng of DNA input from intact or highly fragmented FFPE DNA
  • Satisfy most of your NGS sample prep needs with one streamlined and flexible solution
  • Use single/duplex molecular barcodes (MBC) to remove false positives and accurately detect variants down to ≤1% variant allele frequency
  • Minimize index hopping with 384 unique dual indexing
  • Simplify your order experience with the all-inclusive starter kit
  • Use with SureSelect exomes, catalog panels or easily create custom panels with the SureDesign software
  • One easy, parallel workflow for targeted RNA and DNA sequencing using SureSelect XT HS2 chemistry

Product Overview

Links