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Purified recombinant rat CINC-2beta expressed in E. coli.
Rat CINC2 beta (Cytokine Induced Neutrophil Chemoattractant 2 beta) is a member of the CXC subfamily of chemokines which also includes three other rat CXC chemokines (CINC1, CINC2 alpha, CINC3/MIP2). The rat chemokines CINC show sequence similarity to human GROs and mouse MIP2 but not IL8. Mature CINC2 beta shares 63% amino acid sequence identity with CINC1 and 80% identity to CINC3. Rat CINC2 beta cDNA encodes a 68 amino acid residue protein. The mature recombinant protein has a predicted molecular mass of approximately 7.6 kDa. Based on sequence homology, it has been suggested that CINCs are the rat counterpart of the human GROs. CINC2 alpha and CINC2 beta were originally purified as novel neutrophil chemoattractants from the conditioned medium of rat granulation tissue CINC2 proteins represent the major chemokines purified from conditioned medium of granulation tissue or lipopolysaccharide (LPS) induced inflammatory exudate, though CINC1 and CINC3 are also present. Other cell types known to produce CINC2 proteins include activated macrophages and fibroblasts. Rat CINCs, potent neutrophil attractants and activators, have an important role in the infiltration of neutrophils into inflammatory sites in rats. Recombinant and natural CINC2 proteins are specific neutrophil chemoattractants both in vivo and in vitro. On the basis of cross-desensitization, it has been postulated that rat neutrophils have at least two classes of CINC receptors: a class of CINC3 specific receptor as well as a second common receptor shared by all CINCs.
Our Abpromise guarantee covers the use of ab10367 in the following tested applications.
|WB||Use a concentration of 0.1 - 0.2 µg/ml. Predicted molecular weight: 7.6 kDa.
The detection limit of rat CINC2 beta is approximately 5 ng/lane and 25 ng/lane under non-reducing and reducing conditions, respectively.
|ELISA||Use a concentration of 0.5 - 1 µg/ml.
The detection limit for rat CINC2 beta is approximately 0.5 ng/well.
ab10367 has not yet been referenced specifically in any publications.