Key Features

Checkmark

Sensitive

Limit of detection down to 0.1% VAF

Checkmark

Quantitative

Able to quantify mutation VAF in original sample

Checkmark

Versatile

Applicable to a variety of sample types

Checkmark

Comprehensive

Wide range of mutations covered

Checkmark

User-friendly

Easy workflow

Benefits

  • Detects any mutations in codons 596–601 (c. 1786-1802)
  • Compatible with plasma samples, tumor biopsies, paraffin-embedded sections (FFPE), and fresh frozen tumors
  • Requires 10-100 ng cfDNA from blood plasma, or 10-1,000 ng DNA from tissue biopsy
  • Delivers results in 8 hours, with 2.5 hours of hands-on time

Sample Data

BRAF mutation testing

Variant verification by Sanger sequencing

Because NuProbe’s BDA technology enriches the variant allele frequency (VAF) of mutations by over 200-fold, Sanger’s limit of detection of 20% VAF is effectively improved to 0.1% VAF. Sanger sequencing can be applied to confirm the identity of quantities detected and quantitated by qPCR using standard sequencing protocols.

Workflow

Workflow Step 1

Step 1: DNA Extraction

DNA is extracted from clinical samples with commercial extraction kits such as cobas® cfDNA Sample Preparation Kit, QIAamp DNA Blood Mini Kit, GeneRead DNA FFPE Kit.
40 min (40 min hands-on)

Sanger Sequencing Workflow

Step 2: qPCR BDA Reaction

NuProbe’s qPCR/Sanger kit reagents and clinical samples are prepared for qPCR reactions. After running the reaction, Ct results and BDA products are obtained.
1.5 hrs (30 min hands-on)

Workflow Step 3

Step 3: Sanger Sequencing

BDA products are prepared for Sanger sequencing, including PCR product purification, cycle sequencing and sequencing clean-up.
3.5 hrs (1hr hands-on)

Purified Sanger products are analyzed by capillary electrophoresis.
2 hrs (15 min hands-on)

Compatible Instruments

qPCR

qPCR BioRad CFX96

BioRad CFX96


qPCR ABI 7500

ABI 7500


qPCR Cobas z480

Cobas z480

Sanger sequencing

Sanger Sequencing

ABI 3500 Dx Genetic Analyzer

Background

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

BRAF gene is frequently mutated in specific cancers, including melanoma, papillary thyroid cancer, and colon cancer. The most prevalent BRAF mutations detected in these cancer types are missense mutations that introduce an amino acid substitution at valine 600. The presence of these specific mutations can guide treatment with targeted therapies such as TAFINLAR® (dabrafenib), MEKINIST®(trametinib), and ZELBORAF®(vemurafenib).

The VarTrace™ BRAF Assay enables highly sensitive detection and quantification of BRAF mutations for cancer patients. The kit uses NuProbe’s PCR-based Blocker Displacement Amplification (BDA) technology to enable the selective amplification of low abundant sequence variants (SNV and indels) in a background of wildtype DNA. Following PCR enrichment, Sanger sequencing is applied to reveal the identity of the variants.

Request a Quote






Quantity