Información de Contacto

Teknovas Bizkaia
Parque Tecnológico de Bizkaia, Edificio 804
48160 - Derio (Bizkaia)
Tel.34 94 478 11 81
Fax:   +34 94 478 07 70
Teknovas Navarra
C/ Comunidad de la Rioja nº 5
31010 - Barañain (Navarra) Tel. Centralita:+34 948 25 99 05
Fax:+34 948 25 99 07

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Panel de amplicones, Accel-amplicon Plus, Colorectal Panel, 48 reacciones (SWIFT BIOSCIENCES)

Panel de amplicones, Accel-amplicon Plus, Colorectal Panel, 48 reacciones

  • 48 rxns
  • -
  • Disponibilidad:
Accel-Amplicon Plus Colorectal Panel
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Disponibilidad: Entrega inmediata


Descripción & Documentación

The Accel-Amplicon Plus Colorectal Cancer Panel is an NGS multigene panel for variant discovery and screening. It combines content from peer reviewed publications and other sources to offer comprehensive and exon-level hotspot coverage of 16 clinically-relevant colorectal genes. Areas of interest include genes such as AKT1, TP53, PIK3CA, KRAS and NRAS.

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The panel is modular, allowing you to add focused content to achieve your most optimal design. Either combine pre-validated content such as our Lynch Syndrome content or add your own targets.  We’ll work alongside you to design your assay and then Swift will optimize and wet-bench validate its performance before shipping it to you.

    • Referencia:
    • K4AP-CR8048
    • Especificaciones:
    • Comprehensive: Covers 11,000 COSMIC and 3,500 ClinVar mutations and generates targeted libraries compatible with Illumina® sequencing platforms.

      Informative:  Provides CNV detection of ERBB2 and full exon coverage of TP53 with flanking intron/exon boundaries.

      Powerful:  Simultaneous detection of single nucleotide variants (SNV), copy number variants (CNV) and small insertions and deletions (indels), all within a fast and easy single-tube assay workflow.

      Flexible:  Add our Lynch Syndrome pre-validated content or your own targets using our pre-validated primers or other content. The possibilities are endless.

    • Caracteristicas:
      • Robust performance on cell-free DNA and FFPE samples starting with as little as 10 ngrams input.
      • Highly sensitive detection of rare variants down to 1% allele frequency.
      • Easy, single-tube assay with sequence ready libraries in under 2 hours.
      • Streamlined analysis with new bioinformatics tools including Primerclip or Genialis.
      • Compatible with all Illumina sequencers
    • Categoría de Producto:
    • Paneles de amplicones
    • Capacidad/Volumen:
    • 48 rxns
    • Disponibilidad:
    • Disponible bajo pedido
    • Aplicaciones:
    • Next-Generation Sequencing (NGS)