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In May 2006 CLINIQA obtained the highest level of ISO certification awarded  to IVD companies.

The ISO 13485 is an International Standard for Quality Systems more rigorous than ISO 9001 and designed for medical device manufacturers.
Corporate
C-Reactive Protein (CRP) Control


C-Reactive Protein (CRP) Control
C-Reactive Protein (CRP), 18-22 mg/dL
Prepared from human plasma and pleural fluid the control contains 20 mg/dL ± 10%. Total protein 4-8 g/dL, Biuret method. pH 7.1 ± 0.1. 0.2 µm filtered.
C-Reactive Protein (CRP), Level 1
Prepared from human plasma and human pleural fluid the control contains 0.04-0.06 mg/dL ± 20%. Total protein 4-6 g/dL, Biuret method. PH 7.0 ± 0.2. 0.2 µm filtered.
C-Reactive Protein (CRP), Level 2
Prepared from human plasma and human pleural fluid the control contains 0.15 mg/dL ± 20%. Total protein 4.5-6.5 g/dL, Biuret method. PH 7.2 ± 0.2. 0.2 µm filtered.
C-Reactive Protein (CRP), Level 3
Prepared from human plasma and human pleural fluid control contains 0.8 mg/dL ± 10%. Total protein 4.5-6.5 g/dL, Biuret method. pH 7.2. ± 0.2. 0.2 µm filtered.
C-Reactive Protein (CRP), 40 mg/dL
Prepared from human plasma and pleural fluid, the CRP control contains 40 mg/dL CRP ± 10%. Total protein: 4.5-6.5 g/dL, Biuret method. pH 7.1 ± 0.1. 0.2 µm filtered.
C-Reactive Protein (CRP) Diluent
Prepared from human plasma, the CRP diluent is intended for making intermediate dilutions of CRP controls and calibrators. Total protein: 4.5-6.5 g/dL, Biuret method. 0.2 µm filtered.




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