FMF.5-RT50

FMF 5 Mutation Detection Kit

Quantity: 50 Tests

£815.00

The FMF 5 Mutation Detection Kit utilizes allele-specific PCR technology to accurately identify five key mutations associated with Familial Mediterranean Fever (FMF): E148Q, M694V, V726A, M680I (G/C), and P369S. Compatible with all real-time PCR devices capable of melting curve analysis and CE-IVD certified, this kit offers a comprehensive solution for the diagnosis of FMF, an autosomal recessive disorder characterized by recurrent fever and inflammatory episodes.

The FMF 5 Mutation Detection Kit utilizes allele-specific PCR technology to accurately identify five key mutations associated with Familial Mediterranean Fever (FMF): E148Q, M694V, V726A, M680I (G/C), and P369S. Compatible with all real-time PCR devices capable of melting curve analysis and CE-IVD certified, this kit offers a comprehensive solution for the diagnosis of FMF, an autosomal recessive disorder characterized by recurrent fever and inflammatory episodes.

  • Allele Specific PCR Technology: Ensures precise detection of critical FMF-associated mutations.
  • Broad Compatibility: Usable with any real-time PCR system capable of melting curve analysis, facilitating widespread use.
  • CE-IVD Certification: Meets European standards for in vitro diagnostic medical devices, ensuring reliability and quality.
  • Accurate Diagnosis: Provides reliable identification of FMF-associated mutations, aiding in the accurate diagnosis of the disease.
  • Ease of Use: Simplified testing process allows for quick and easy identification of the FMF mutations through a multiplex PCR approach.
  • Versatile Use: The kit’s compatibility with various real-time PCR devices enhances its utility across different laboratory settings.
  • Diagnosis of Familial Mediterranean Fever: Specifically designed for detecting mutations associated with FMF, this kit is crucial for diagnosing individuals experiencing recurrent fever and inflammatory symptoms, particularly those of Turkish, Arab, Armenian, and Sephardic Jewish descent.
  • Carrier Screening: Useful in identifying carriers of FMF mutations within high-prevalence populations, aiding in genetic counseling and disease management.
  • Mutation Coverage: Targets the E148Q, M694V, V726A, M680I (G/C), and P369S mutations linked to FMF.
  • Technology: Utilizes multiplex PCR for targeted detection of FMF-associated genetic variations.
  • Compatibility: Suitable for all real-time PCR instruments capable of conducting melting curve analysis.
  • Certification: Carries the CE-IVD mark, indicating its suitability for in vitro diagnostic use within the European Union.

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