Human C-Reactive Protein (CRP) ELISA Kit (IVDIA1000-FA)

Regulatory status: For research use only, not for use in diagnostic procedures.

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Intended Use
C-Reactive Protein (CRP) ELISA Kit is a quantitative solid phase enzyme linked immunosorbent assay. This test provides quantitative measurement of human C-Reactive Protein in serum to aid in the follow up of rheumatic fever, inflammatory processes, myocar.
Contents of Kit
1. Micro-wells strips (96 wells)
2. Sample Diluent or zero standard (50 mL)
3. Enzyme conjugate (11 mL)
4. Reference Standard Set (0.3 mL each vial)
5. TMB Solution (11 mL)
6. Washing buffer Concentrate (100x) (10 mL)
7. Stop Solution
8. Well holder
1. Store the kit at 2-8°C in a refrigerator. Keep micro-wells sealed in dry bag with desiccants.
2. The unopened reagents are stable until expiration of the kit.
3. TMB Solution should be colorless; if the solution turns blue, it must be replaced.
Intra-assay: Eleven samples each from three pooled sera were assayed in a single run. Inter-assay: Three pooled sera were assayed in duplicate in four days.
0.35 ng/mL
General Description
C-Reactive Protein (CRP) has been regarded as an acute-phase reactant in serum. It consists of five single subunits with a molecular weight of 23,000, each noncovalently linked and assembled as a cyclic pentamer with a molecular weight range from 110,000 to 140,000 CRP has been found to be present in increased amounts in serum of patients with a wide variety of diseases including infections by gram-positive and gram-negative organisms acute phase of rheumatoid arthritis, myocardial infarction, malignant tumors abdominal abscesses, peritonitis, and inflammation of the bile duct. Less consistently, CRP may be found in patients with Guillain-Barre Syndrome and multiple sclerosis: in active tuberculosis acute infectious hepatitis, and certain viral infections; in many other necrotic and inflammatory diseases: in burned patients; and after surgery trauma.
Although the detection of elevated levels of CRP in the serum is not specific for any particular disease, it is a useful indicator of inflammatory processes. CRP levels rise in serum within hours of the onset of inflammation, reaching a peak during the acute stage and decreasing with the resolution of inflammation or trauma. The detection of CRP is a more reliable and sensitive indicator of the inflammatory process than the erythrocyte sedimantation rate (ESR), which may also be influenced by physiological changes not associated with an inflammatory process. Current quantitation methods including nephelometry, latex agglutination, radial immunodiffusion have the general disadvantages accompany agglutination and precipitation techniques.


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