HDL-C L-Type Assay

Description

HDL-C L-Type Assay is an in vitro diagnostic (IVD) test for the quantitative determination of High Density Lipoprotein Cholesterol (HDL-C) in serum.

HDL-C is an important tool used to assess the individual risk of developing coronary heart disease (CHD) since a strong negative relationship between HDL-C concentration and CHD was reported.

HDL-C L-Type Assay is a liquid type reagent that assays HDL-C in serum by blocking lipoproteins like LDL, VLDL and chylomicrons (immunoinhibition method) and subsequent enzymatic reactions.

Reagent 1, Reagent 2 and a calibrator are required for this assay.
OEM test components are available for this assay.

All reagents and calibrators are CE-certified according to Directive 98/79/EC on in vitro diagnostic medical devices.

Key Features

  • High stability of ready-to-use reagents
  • Within-run imprecision: < 1%
  • Total precision (NCCLS EP5-T2): < 1.5%
  • No interference by other serum components
  • Excellent correlation to the CDC reference method DCM (Designated Correlation Method)
  • Also available as bulk

Storage

Store at 2-10° C. Do not freeze reagents.

Safety information

Health Hazard

Downloads

Ready-to-use Test Components
OEM Test Components