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Cepheid Xpert FII & FV

Cepheid Xpert FII & FV

Product Details:

  • Features Rapid, Accurate, Fully automated, Minimal hands-on time
  • Usage Type Clinical Diagnostic
  • Function Simultaneous detection of Factor II (FII) and Factor V (FV) gene mutations
  • Accuracy >99% for mutation detection
  • Measurement Range Qualitative polynucleotide detection
  • Frequency Run as required
  • Instruments Type For use with GeneXpert Systems
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Cepheid Xpert FII & FV Price And Quantity

Cepheid Xpert FII & FV Product Specifications

  • Detection and differentiation of FII/FV gene polymorphisms
  • Run as required
  • No
  • New
  • Real-Time PCR (Polymerase Chain Reaction)
  • Approx. 750g (kit)
  • Clinical Diagnostic
  • Reagent kit with consumables
  • Rapid, Accurate, Fully automated, Minimal hands-on time
  • As per GX instrument specifications
  • White/Yellow labeling (varies by batch)
  • >99% for mutation detection
  • Simultaneous detection of Factor II (FII) and Factor V (FV) gene mutations
  • Qualitative polynucleotide detection
  • Yes (kit is transportable; used with GX system)
  • 12 months from manufacturing
  • Kit packaging: 230 mm x 170 mm x 80 mm approx.
  • Automated
  • Instrument-based digital (via GeneXpert display)
  • 2C - 28C, do not freeze
  • Molecular Diagnostic Assay
  • Yes
  • Low
  • Electrical (via instrument)
  • As per GX instrument specifications
  • For use with GeneXpert Systems
  • Minimal; on-screen prompts provided by system
  • High; validated for clinical diagnostics of FII/FV
  • Internal controls included in cartridge
  • 1 mL (whole blood); 50 µL (purified DNA)
  • High; distinguished FII G20210A and FV Leiden mutations
  • Single cartridge per test, scalable with instrument module
  • GeneXpert IV, GeneXpert XVI, GeneXpert Infinity series
  • Whole blood or purified genomic DNA
  • ~40 minutes per sample
  • Cartridge kits, Reagent kits, Instructions for Use

Cepheid Xpert FII & FV Trade Information

  • 100 Unit Per Week
  • 7 Days

Product Description

Brand Cepheid
Product Type PCR Kit
Sample Type 10T
CAT No GXFIIFV-10
Application Molecular Biology

Xpert FII & FV is a qualitative genotyping test for the rapid detection of Factor II (FII) and Factor V (FV) alleles. Performed on the Cepheid GeneXpert System, the test is intended to provide rapid results for Factor II c.*97G>A (G20210A) and Factor V Leiden c.1601G>A (G1691A or R506Q) mutations as an aid in the diagnosis of suspected thrombophilia.



Effortless Mutation Detection

The Xpert FII & FV assay utilizes automated real-time PCR technology to accurately differentiate and detect FII and FV gene mutations. Its cartridge format with internal quality controls guarantees reliability, enabling clinical professionals to obtain results with minimal hands-on time.


Flexible Sample Processing

Sample volume requirements are adaptable to either whole blood (1 mL) or purified genomic DNA (50 L), making this system versatile for both routine and specialized diagnostic testing. The kit's compact size and portability support easy workflow integration in various clinical settings.


Reliable and Rapid Operation

Compatible with GeneXpert IV, XVI, and Infinity systems, the assay delivers high-throughput results as needed. Each test cycle is completed in about 40 minutes, empowering clinicians to make timely decisions for patient care.

FAQ's of Cepheid Xpert FII & FV:


Q: How does the Cepheid Xpert FII & FV assay work for detecting gene mutations?

A: The assay employs automated real-time PCR to simultaneously detect Factor II (FII) and Factor V (FV) gene mutations, specifically the FII G20210A and FV Leiden. The system processes either whole blood or purified DNA samples in a single-use cartridge, generating high-accuracy results.

Q: What sample types and volumes are required for running the test?

A: You can use either whole blood (1 mL) or purified genomic DNA (50 L) as sample input. This flexible approach accommodates different laboratory workflows and patient sample availability.

Q: When is the Xpert FII & FV recommended for use in clinical diagnostics?

A: The test is recommended whenever detection and differentiation of FII and FV-related gene polymorphisms are required, especially in clinical diagnostics for thrombophilia and related conditions. Its rapid turnaround time supports urgent and routine diagnostic needs.

Q: Where can I operate this molecular assay, and is it portable?

A: The Xpert FII & FV kit can be operated in any clinical or laboratory setting equipped with GeneXpert systems (IV, XVI, or Infinity series). While the kit itself is transportable, its use requires a compatible instrument.

Q: What processes are involved from sample to result?

A: After loading the sample into the cartridge and inserting it into the GeneXpert instrument, the assay runs fully automated, guided by on-screen prompts. Internal controls within the cartridge ensure integrity, and test completion occurs in about 40 minutes.

Q: What are the benefits of using Cepheid Xpert FII & FV assay?

A: Benefits include rapid, reliable, and highly specific detection of clinically significant gene mutations with greater than 99% accuracy, minimal hands-on time, and streamlined workflow suitable for scalable clinical laboratories.

Q: Is user training required before operating the assay system?

A: Minimal user training is necessary, as the instrument provides digital, on-screen prompts throughout the testing process. Comprehensive instructions for use are included in the kit.

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