CRP / C-Reactive Protein Antikörper (Antigen Affinität reinigt)

11.02.2012

Produkt-Information von CRP / C-Reactive Protein Antikörper

Immunogen	Recombinant Rat CRP / C-Reactive Protein protein (Catalog#80041-R08H)
Antibody Type	Rabbit Polyclonal Antibody ( Antibody Purification Platform )
Ig Type	Rabbit IgG
Formulation	0.2 μm filtered solution in PBS with 5% trehalose

CRP / C-Reactive Protein Antikörper Usage Guide

Specificity	Rat CRP / C-Reactive Protein
Western blot	This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Rat CRP in WB. Using a DAB detection system, the detection limit for Rat CRP is approximately 1 ng/lane under non-reducing conditions and reducing conditions.
Direct ELISA	This antibody can be used at 0.1-0.2 μg/mL with the appropriate secondary reagents to detect Rat CRP. The detection limit for Rat CRP is approximately 0.00975 ng/well.
Storage	This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free. Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.

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Hintergrund von CRP / C-Reactive Protein Antikörper

C-reactive protein (CRP) is synthesized by the liver in response to factors released by fat cells. It is a member of the pentraxin family of proteins. The levels of CRP rise in response to inflammation. Human C-reactive protein (CRP) is the classical acute phase reactant, the circulating concentration of which rises rapidly and extensively in a cytokine-mediated response to tissue injury, infection and inflammation. Serum CRP values are routinely measured, empirically, to detect and monitor many human diseases. However, CRP is likely to have important host defence, scavenging and metabolic functions through its capacity for calcium-dependent binding to exogenous and autologous molecules containing phosphocholine (PC) and then activating the classical complement pathway. CRP may also have pathogenic effects and the recent discovery of a prognostic association between increased CRP production and coronary atherothrombotic events is of particular interest.

References

Pepys MB. et al., 2003, J Clin Invest. 111 (12): 1805-12.
Thompson D. et al., 1999, Structure. 7 (2): 169-77.

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