Breast cancer NGS panel

An easy-to-use kit containing all of the components necessary to make library for next generation sequencing on Illumina or Ion Torrent platforms. The kit provides comprehensive coverage of:


96 samples (Illumina) $7,020.00

Cat no. NGS-BRCA1/2-IL-96

96 samples (Illumina) $7,020.00

Cat no. NGS-BRCA1/2-IL-96

8 samples (Illumina) $585.00

Cat no. NGS-BRCA1/2-IL-8

96 samples (IonTorrent) $7,020.00

Cat no. NGS-BRCA1/2-IT-96

8 samples (IonTorrent) $585.00

Cat no. NGS-BRCA1/2-IT-8

Available for direct shipping to United States.

Watch this space for a fully automated analysis solution to accompany this kit. This tool is in development. Our data analysis tools turn your NGS data in to useful, actionable answers. Please email us for more details.
Complete kit containing all necessary reagents:

- Multiplex primers for PCR1
- All PCR mastermixes required
- All clean-up beads and reagents
- Indexes/adapters for PCR2
Analysing somatic mutations in the BRCA genes can help to define clinical strategy for treatment of breast and ovarian cancer. Whereas detection of germline BRCA mutations can support decision making on risk reduction strategies such as hormone replacement therapy, chemoprevention strategies and prophylactic surgery.
Our simple to use PCR driven kit generates an ideal library for full and uniform coverage of BRCA1 and BRCA2, covering all exons and exon/intron junctions. The kit uses overlapping amplicons to ascertain superior INDEL coverage be used to detect both germline and somatic mutations.

Your Questions Answered

Upon receipt, store the kit at -20°C. When stored and handled correctly, the kit components will remain perfect for at least six months from the date of receipt. All components of the kit – are stable for more than 20 freeze/thaw cycles.
A collection of DNA or cDNA fragments prepared for sequencing by a performing a series of enzymatic steps. These steps are commonly referred to as the Library Preparation.
- Single-End Read (SE), which provides sequence from only one end of the DNA insert - Paired-End Read (PE), which provides sequence from both ends of a DNA insert - Mate Pair Read (ME), Similar to paired-end but both reads come from a single strand of DNA

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