Cepheid Xpert FII & FV

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Product Details:

Accuracy >99% for mutation detection
Measurement Range Qualitative polynucleotide detection
Instruments Type For use with GeneXpert Systems
Storage Instructions 2°C - 28°C, do not freeze
Display Type Instrument-based digital (via GeneXpert display)
Usage Type Clinical Diagnostic
Frequency Run as required
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Cepheid Xpert FII & FV Price And Quantity

Cepheid Xpert FII & FV Product Specifications

Operating Type Automated
Usage Type Clinical Diagnostic
Frequency Run as required
Technology Real-Time PCR (Polymerase Chain Reaction)
Portable Yes (kit is transportable; used with GX system)
Wall Mounted No
Power Source Electrical (via instrument)
Real-Time Operation Yes
Function Simultaneous detection of Factor II (FII) and Factor V (FV) gene mutations
Shelf Life 12 months from manufacturing
Features Rapid, Accurate, Fully automated, Minimal hands-on time
Power Consumption As per GX instrument specifications
Equipment Type Molecular Diagnostic Assay
Color White/Yellow labeling (varies by batch)
Dimension (L*W*H) Kit packaging: 230 mm x 170 mm x 80 mm approx.
Voltage As per GX instrument specifications
Measurement Range Qualitative polynucleotide detection
Accuracy >99% for mutation detection
Display Type Instrument-based digital (via GeneXpert display)
Condition New
Use Detection and differentiation of FII/FV gene polymorphisms
Material Reagent kit with consumables
Instruments Type For use with GeneXpert Systems
Noise Level Low
Storage Instructions 2°C - 28°C, do not freeze
Weight Approx. 750g (kit)

Specificity High; distinguished FII G20210A and FV Leiden mutations
Sample Volume 1 mL (whole blood); 50 µL (purified DNA)
Throughput Single cartridge per test, scalable with instrument module
Quality Control Internal controls included in cartridge
Test Time ~40 minutes per sample
User Training Minimal; on-screen prompts provided by system
Package Contents Cartridge kits, Reagent kits, Instructions for Use
Sample Type Whole blood or purified genomic DNA
Sensitivity High; validated for clinical diagnostics of FII/FV
Compatible Instruments GeneXpert IV, GeneXpert XVI, GeneXpert Infinity series

Cepheid Xpert FII & FV Trade Information

Supply Ability 100 Unit Per Week
Delivery Time 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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