OptiQnt Clinical Chemistry Kit

QptiQnt series is ready-to-use liquid clinical chemistry reagents delivering precise, reliable results across routine biochemical testing applications.

SKU: NCC0472010 Categories: ,

Description

Description

The clinical chemistry range offers reagents and assays for the quantitative analysis of biochemical markers in bodily fluids.

Key Features
  • Universal compatibility
  • Consistent sensitivity and linearity
  • Extended shelf life
  • Liquid stable reagents
  • GMP regulation compliant
  • Competitive pricing
  • Comprehensive coverage

General Specifications

  • Product Type: Ready-to-use liquid clinical chemistry reagents
  • Intended Use: Quantitative determination of routine biochemical parameters in human serum, plasma or urine, using semi-automated and fully automated clinical chemistry analysers

General Characteristics

  • Format: Liquid stable, ready-to-use reagents
  • Methodology: Colorimetric/enzymatic/kinetic (parameter dependent)
  • Instrument Compatibility: Open system; suitable for all major semi-automated and automated clinical chemistry analysers
  • Specimen Type: Serum, plasma urine (parameter dependent)
  • Assay Principle: Enzyme-substrate reaction with spectrophotometric endpoint measurement
  • Measuring Wavelength: 340–750 nm (depending on parameter)
  • Linearity Range: Broad linearity with reduced need for repeat dilutions (parameter specific, e.g.,
    glucose up to 500 mg/dl)
  • Stability:
    • Unopened vial: 14–24 months at 2–8°C
    • Opened vial: Typically 30–60 days at 2–8°C (parameter dependent)
  • Packaging Sizes: 2 × 50 ml, 4 × 50 ml, 2 × 100 ml, 4 × 100 ml, 10 × 100 ml (customized pack sizes available)
  • Controls and Calibrators: Compatible with NGIVD’s multi-parameter controls and calibrators

Performance Characteristics

  • Precision: CV% ≤5% intra- and inter-assay variation
  • Accuracy: Correlation ≥0.98 with reference/gold-standard methods
  • Sensitivity: Optimised detection limits to cover clinical decision ranges
  • Interference: Minimal effect from hemolysis, icterus, or lipemia (verified per)
  • Reagent Blank: Provided where applicable