C-reactive protein (CRP) in serum/plasma

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Indications

Reference interval

# reference values are race & gender-dependent[13] mean CRP 3.0 mg/L blacks vs 2.3 whites, 3.3 women vs 1.8 men

* high-sensitivity CRP in serum used for assessing cardiovascular risk; use average of 2 measurements; 2 weeks apart (see guidelines for high-sensitivity CRP testing)

Principle

The CRP pack is used in the DuPont ACA discrete clinical analyzer to quantitatively measure C-Reactive protein levels in serum. The C-Reactive Protein (CRP) method is based on a particle enhanced turbidimetric immunoassay (PETIA) adapted to the DuPont ACA analyzer. The CRP method uses a single-pack, rate technique to measure C-reactive protein. The CRP pack contains latex particles coated with the antibody to C-reactive protein (AbPR). C-reactive protein present in the sample causes aggregation of the latex particles. The rate of aggregation is directly proportional to the concentration of C-reactive protein and is measured turbidimetrically at 340 nm. The concentration is determined by means of a previously prepared lot-specific calibration curve or mathematical function.

Clinical significance

Increases

Specimen

Patient preparation: No special patient preparation is required. Collect blood samples by venipuncture following established good laboratory practices. If the sample is obtained through the infusion set, flush the line thoroughly with saline before taking the blood sample.

More general terms

More specific terms

Additional terms

Component of

References

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Patient information

C-reactive protein (CRP) in serum patient information