Features
• >95% overall agreement with predicate method for accurate assessment of patients at risk of progression to severe sepsis and septic shock
• State-of-the art sensitivity and low-end precision―20% CV LoQ of 0.02 ng/mL and CV ≤8% at concentrations of ≥0.150 ng/mL
• Rapid access to results with first result in approximately 20 minutes
• Minimal sample draw of 35 µl pick-up volume
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Specifications
• Sample type / size: Serum, plasma (lithium heparin) / 35 μL
• Approximate calibrator levels: 0, 0.8, 5, 10, 25, 50 and 100 ng/mL (μg/L)
• Analytical measuring range: 0.01–100 ng/mL (μg/L), up to 1,000 ng/mL with Special Dilution Feature
• Limit of Detection (LoD): 0.01 ng/mL (μg/L)
• 20% CV Limit of Quantitation: 0.02 ng/mL (μg/L)
• Imprecision: Total imprecision ≤8.0% CV at concentrations ≥0.150 ng/mL, and standard deviation (SD) ≤0.012 ng/mL at concentrations <0.150 ng/mL
• Open pack stability: 42 days
• Calibration stability: 42 days
• Time-to-first result (approx.): 20 minutes
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