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N Latex CDT Assay

Highly specific screening for detection of chronic alcohol abuse

Assay principleLatex-enhanced immunonephelometry
Sample typeHuman serum
Measuring time18 minutes
Reference range28.1–76 mg/L (1.19–2.47% CDT)*
Initial measuring range20–660 mg/L
Once-opened reagent stability2 weeks on BN ProSpec® System
3 days (6 days with evaporation stoppers) on BN™ II System
Calibration frequency2 weeks
PrecisionRepeatability: <4.5%
Within-lab: <2.0%

*%CDT results determined with N Latex CDT assay in concurrence with N antiserum to human transferrin (1st to 99th percentile)

The products/features shown on this web page are not commercially available in all countries. Due to regulatory reasons their future availability cannot be guaranteed. Please contact your local Siemens organization for further details.

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