FMF-RT50

FMF 11 Mutation Detection Kit

Quantity: 50 Tests

£1,778.00

The FMF 11 Mutation Detection Kit is engineered to identify 11 specific mutations associated with Familial Mediterranean Fever (FMF): E148Q, M694V, V726A, M680I (G/C), K695R, R408Q, M694I, R761H, P369S, F479L, and A744S. Utilizing allele-specific PCR technology, this kit ensures accurate results and is compatible with all real-time PCR devices capable of melting curve analysis. With its CE-IVD certification, it offers a reliable solution for diagnosing FMF, an autosomal recessive disorder known for causing recurrent fever and inflammation, particularly affecting populations in the Mediterranean region.

  • Allele Specific PCR Technology: Guarantees precise detection of a broad range of FMF-related mutations.
  • Comprehensive Mutation Coverage: Includes 11 mutations for a thorough assessment of the genetic basis of FMF.
  • Universal Device Compatibility: Designed to work with any real-time PCR system equipped for melting curve analysis, providing flexibility across different laboratory setups.
  • CE-IVD Certification: Adheres to European standards for in vitro diagnostic medical devices, affirming the kit’s quality and dependability.
  • Diagnosis of Familial Mediterranean Fever: Essential for identifying individuals with FMF, aiding in the early diagnosis and management of the disorder, especially among high-risk populations like Turks, Arabs, Armenians, and Sephardic Jews.
  • Genetic Screening and Carrier Detection: Facilitates carrier screening within communities with high FMF prevalence, contributing to better disease understanding and management strategies.
  • Mutation Coverage: Targets 11 key mutations (E148Q, M694V, V726A, M680I (G/C), K695R, R408Q, M694I, R761H, P369S, F479L, A744S) linked to FMF.
  • Technology: Employs multiplex PCR for targeted detection of genetic variations associated with FMF.
  • Compatibility: Compatible with all real-time PCR devices capable of conducting melting curve analysis.
  • Certification: CE-IVD marked, ensuring compliance with EU regulations for in vitro diagnostic use.

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