Lumipulse® G β-Amyloid Ratio (1-42/1-40) CSF

The Lumipulse G  β-Amyloid Ratio (1-42/1-40) is an in vitro cerebral spinal fluid (CSF) test that combines the results of Lumipulse G  β-Amyloid 1-42 and Lumipulse G  β-Amyloid 1-40 into a ratio of ß-Amyloid 1-42 to ß-Amyloid 1-40 concentration using the LUMIPULSE G1200. 

For in vitro diagnostic use
Lumipulse® G β-Amyloid 1-42 IRC

Product # 231432

3 x 14 Cartridges
Lumipulse® G β-Amyloid 1-42 Calibrators

Product # 234884

2 x 3 Concentrations
Lumipulse® G β-Amyloid 1-40 IRC

Product # 231753

3 x 14 Cartridges
Lumipulse® G β-Amyloid 1-40 Calibrators

Product # 234891

2 x 3 Concentrations
Lumipulse® β-Amyloid Controls

Product # 234907

2 x 3 Concentrations
Lumipulse G β-Amyloid 1-40 Immunoreaction Cartridges (231524) and Lumipulse G β-Amyloid 1-40 Calibrators (231531) Lumipulse G β-Amyloid 1-42 Immunoreaction Cartridges (230336) and Lumipulse G β-Amyloid 1-42 Calibrators (230343)

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    Please note: precaution

    The Lumipulse G β-Amyloid Ratio (1-42/1-40) must be calculated using the results obtained from Lumipulse G β-Amyloid 1-42 and Lumipulse G β-Amyloid 1-40 on the same patient sample and same LUMIPULSE G1200 Analyzer. Use of another manufacturer's assays may result in significantly different ratios. β-amyloid 1-42 and β-amyloid 1-40 values determined on patient samples using other manufacturers’ assays cannot be interchangeably used to calculate the Lumipulse G β-Amyloid Ratio (1-42/1-40) which could lead to wrong diagnostic conclusions. The Lumipulse G β-Amyloid 1-42 assay should only be used with the Lumipulse G β-Amyloid 1-40 to calculate the ratio of β-amyloid 1-42 / β-amyloid 1-40. The Lumipulse G β-Amyloid 1-42 and Lumipulse G β-Amyloid 1-40 assays are not intended to be used individually.

     

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  • Citations

    The BIOZ badges associated with Fujirebio products include peer-reviewed citations derived from scientific studies using Fujirebio products. Please note that the peer-reviewed citations do not reflect the regulatory status of Fujirebio products. Users should refer to the specific product documentation and any (clinical) claims made therein in order to ensure compliant use. For each country or geographic region, users must verify the related regulatory status of the Fujirebio product.

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