Code | CSB-AP000641HU |
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Size | $354 |
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our Recombinant Human CXCL2 protein is an indispensable research tool for investigators focusing on immunology. This C-X-C motif chemokine 2 protein, also known by its aliases CXCL2, GRO2, GROB, MIP2A, and SCYB2, is expressed in E. coli and covers the 35-107aa region, encompassing the full length of the mature protein. This tag-free, lyophilized powder can be easily reconstituted with sterile water or an appropriate buffer to meet various experimental requirements.
Our Recombinant Human CXCL2 protein exhibits a high purity of >97%, as confirmed by both SDS-PAGE and HPLC analyses. The endotoxin levels are stringently controlled, ensuring they remain below 1.0 EU/µg, as verified by the LAL method. The protein is fully biologically active when compared to standard, with its biological activity determined by a chemotaxis bioassay using human CXCR2 transfected human 293 cells within a concentration range of 10-100 ng/ml.
The significance of CXCL2 in immunology research is well documented. For instance, Zhou et al. (2001)[1] demonstrated the importance of CXCL2 in neutrophil infiltration and activation during acute inflammation, providing insights into the chemokine's potential therapeutic applications. In another study, Sugimoto et al. (2012)[2] reported the potential anti-inflammatory effects of CXCL2 inhibition in experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis, further emphasizing the protein's relevance in understanding immune system function and developing potential treatments for immune-related disorders.
References:
1. Zhou H, et al. Neutrophil infiltration and activation in bronchoalveolar lavage fluid from patients with acute respiratory distress syndrome: a role for C-X-C chemokine. Chin Med J (Engl). 2001;114(2):174-8.
2. Sugimoto K, et al. Inhibition of C-X-C chemokine receptor 2 (CXCR2) suppresses EAE development by suppressing accumulation of neutrophils and macrophages in the CNS, and subsequent demyelination. Nihon Rinsho Meneki Gakkai Kaishi. 2012;35(5):424-33.
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