DPYD Multiplex Set gDNA

SKU: CC-SID-000110 Category: Tag:

Product Description

Reference materials for Pharmacogenetics (PGx)

SensID has developed a totally platform agnostic control for dihydropyrimidine dehydrogenase (DPYD; DHP; DPD; DHPDHASE) testing. The implemented variants were selected based on publications and suggestions of various working groups and key opinion leaders who support the implementation of DPYD testing. Authorities like EMA and NHS are recommending that all patients have to be tested for DPYD deficiency prior to systemic therapy with the FU-containing drugs 5-fluorouracil (5-FU), Capecitabine, Tegafur and Flucytosine. This product consist of a set of gDNA at either 0%, 50% or 100% mutated gene with a highly characterized genomic background. Mutations in this gene result in DPYD deficiency, an error in pyrimidine metabolism associated with thymine-uraciluria and an increased risk of toxicity in cancer patients receiving 5-fluorouracil chemotherapy.

Therapeutic indications where DPYD mutation status is relevant:

  • colorectal cancer
  • gastric cancer, pancreatic cancer, oesophageal cancer
  • breast cancer
  • squamous cell carcinoma of the head and neck
  • biliary tract cancers
  • Non–small-cell lung cancer (NSCLC)
  • Systemic yeast and fungal infections due to sensitive organisms

This product is ideal for Next Generation Sequencing (NGS) workflows. In particular:
– Validation and development of sequencing protocols (e.g. Whole Genome Sequencing (WES), Amplicon Sequencing) and PCR protocols
– Calibration and development of instruments and workflows in DNA processing (e.g. DNA fragmentation via acoustic shearing, enzymatic digestion or sonication)
– Analyze the performance of your NGS pipeline by comparing to freely available datasets

Unit Size: 1000 ng per vial (3 vials in total)

Concentration: 10 ng/µl

Included mutations (ddPCR validated):

rsnumber HGVS Nomenclature Allelic frequency
vial 1 vial 2 vial 3
rs56038477    c.1236G>A 0% 50% 100%
rs56276561    c.483+18G>A 0% 50% 100%
rs67376798    c.2846A>T 0% 50% 100%
rs75017182    c.1129–5923C>G 0% 50% 100%
rs55886062    c.1679T>G 0% 50% 100%
rs3918290    c.1905+1G>A 0% 50% 100%
rs72549309    c.295_298delTCAT 0% 50% 100%
rs115232898    c.557A>G 0% 50% 100%
rs1801160    c.2194G>A 0% 50% 100%

Further variants were investigated. See “additional mutations covered”.

Buffer: Tris-EDTA (10 mM Tris, 1 mM EDTA), pH 8,0

Storage: 2-8 °C

Expiry: stable for 24 months from date of manufacture (as supplied)

Quality control

Fragmentation size: Agarose Gel-Electrophoresis

Allelic Frequency (metrologically traceable): ddPCR

Quantification (metrologically traceable): Fluorometric dsDNA measurement (QuBit)

Technical background

Derived from: SensID proprietary cell line

Bioinformatics: Whole Exome Sequencing (WES) data available on request.

Indication:   Research Use Only

Manufactured by:  SensID GmbH

Product documentation, such as certificates of analysis, and additional technical support is available directly from the manufacturer of this product.
Click the link below to visit their website.

Documents and Support for this product at SensID

Shopping Cart
Scroll to Top