LAMP Human DPD Deficiency KIT - DPYD*6
The LAMP Human DPD6 KIT is an in vitro diagnostic test intended for the qualitative detection of the less functional DPYD allele *6 by Loop-mediated isothermal amplification (LAMP).
This assay is dedicated to professional use in diagnostic laboratories. The device is not for self-testing.
Regulatory Status: RUO
Format: 24 reactions
Target gene: DPYD
Drug relevance: Fluoropyrimidines, including drugs like 5-fluorouracil (5-FU), capecitabine, and tegafur
Variants detected: DPYD*6 (rs1801160)
Method: LAMP + meting curve analysis
Sample: EDTA whole blood - no DNA extraction required - or extracted DNA
Compatible instruments: LightCycler 480 I&II / Cobas z 480 (Roche); CFX96 / CFX Opus 96 (Bio-Rad); QuantStudio 1/3/5 & 6/7 Flex (Applied Biosystems); MIC qPCR (Bio Molecular Systems); LC-Genie III & Genie HT (Optigene)
Turn around time: < 1h
General information
Advantages
Linked products
The assay with the “LAMP Human DPD Deficiency KIT-DPYD*6” is performed on whole blood samples either freshly collected or stored at -20°C, or on extracted DNA samples.
The “LAMP Human DPD Deficiency KIT-DPYD*6” contains 6 specific primers allowing the loop-mediated amplification of a specific region surrounding the polymorphism. Each amplified target sequence is detected by a probe through the detection of fluorescence variation. After amplification, the temperature is decreased to 40°C and the probe hybridizes the amplified fragment, bringing the fluorophore and the quencher in proximity, resulting in quenching of the fluorescence. During the melting curve analysis, the temperature is gradually increased while the change in fluorescence emission is measured. The probe will detach differently from amplified wild type DNA fragments and mutated DNA fragments, therefore, the change in fluorescence will be observed at a different temperature, allowing to make the difference between homozygous mutated, heterozygous mutated or wild type for the DPYD*6 allele.
Test principle
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