Ultrasensitive C-Reactive Protein

This product is used on NEPHSTAR® protein analysis system for quantitative determination of human Ultrasensitive C-Reactive Protein (UsCRP) in serum


Catalog No
Product Catalog No: DK025

Pack Size:
Pack Size:
Pack Size:
Pack Size:
Code Name Volume/Quantity
Product Catalog No: DA025 Pack Size: UsCRP Antiserum Pack Size: 1×2.0 ml
Product Catalog No: DB025 Pack Size: UsCRP Reaction buffer Pack Size: 1×25.0 mL
Product Catalog No: DC025 Pack Size: UsCRP Magnetic card Pack Size: 1
Product Catalog No: DM025 Pack Size: UsCRP Control Pack Size: 1×0.5mL

Product Code: UsCRP
Category:
Summary

C-Reactive Protein (CRP) is an acute marker of inflammatory processes. In case of an acute inflammation the concentration of CRP increases and decreases more quickly than the red cell sedimentation rate. The increase of CRP occurs in a non-specific way in different kinds of tissular aggression, as for example in infectious states, rheumatoid arthritis, myocardium infarct, malignant tumour, etc. Routinely available immunochemical assay methods for CRP have limited sensitivity, and until recently, CRP concentrations below 10 mg/L could not be measured precisely, leading to the wide spread adoption of this value as the upper limit of the health-associated reference range. This is satisfactory for most purposes in general medicine. However, in neonatal pediatric practice, a high sensitive CRP immunoassay shows that health-associated reference values are below 1 – 2 mg/L and that any rise above such values is associated with serious disease, usually bacterial infection. More recently, application of sensitive CRP assays to studies of adult cardiovascular disease has revealed important prognostic relationships between modest increase of CRP and the occurrence, progression, and thrombo-occlusive complications of atherosclerosis. We therefore developed an ultra sensitive CRP assay with a detection limit around 1.0 mg/L and a high measuring range (0 – 150 mg/L CRP).

Test Principle

Particle-enhanced immunonephelometry is applied. This method involves measuring the light scattered by insoluble complexes formed by reaction between specific protein in samples and its respective antibody covalently coupled to latex particles, and the amount of scattered light is directly proportional to the concentration of the protein under condition that antiserum is in excess. The latex particles increase the size of complexes formed and thus the amount of light as well as the test sensitivity. Concentrations are automatically calculated by reference to a calibration curve stored in the instrument.

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References

1. Claus DR, Osmand AP, Gewurz H. Radioimmunoassay of human C-reactive protein and levels in normal sera. J Lab Clin Med 1976; 87: 120-128

2. Wasunna A, Whitelaw A, Gallimore R, Hawkins PN, Pepys MB. C-reactive protein and bacterial infection in preterm infants. Eur J Pediatr 1990; 149:424-427

3. Heinrich J, Schulte H, Schönfeld R, Köhler E, Assmann G. Association of variables of coagulation, fibrinolysis and acute-phase with atherosclerosis in coronary and peripheral arteries and those arteries supplying the brain. Thromb Haemostas 1995; 73: 374-379

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