Recombinant Mouse CXCL2 protein (rFc Tag) (HPLC verified)

种属

Mouse

纯度

>90 %, SDS-PAGE
>90 %, SEC-HPLC

标签

rFc Tag

生物活性

未测试

Cat no : Eg2239

Print datasheet

Synonyms

C-X-C motif chemokine 2, Macrophage inflammatory protein 2, MIP2, Mip-2, Scyb2



产品信息

纯度 >90 %, SDS-PAGE
>90 %, SEC-HPLC
内毒素 <0.1 EU/μg protein, LAL method
生物活性
Not tested
来源 HEK293-derived Mouse CXCL2 protein Ala28-Asn100 (Accession# P10889) with a rabbit IgG Fc tag at the N-terminus.
基因ID 20310
蛋白编号 P10889
预测分子量 35.0 kDa
SDS-PAGE 34-38 kDa, reducing (R) conditions
组分 Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
复溶 Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
储存条件
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
运输条件 The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

背景信息

CXCL2, also known as macrophage inflammatory protein 2-alpha (Mip2-alpha), is a member of CXC chemokine family that binds to CXC chemokine receptor 2 (CXCR2). CXCL2 is mainly produced by macrophages, endothelial cells, epithelial cells and tumor cells. CXCL2 plays important roles in various biological progresses such as angiogenesis, inflammation, immune response and cancer biological behaviors. Under inflammatory conditions in CNS, microglia and astrocytes may secrete CXCL2 as well as other chemokines, which induces chemotaxis and infiltration of circulatory neutrophils. Indeed, previous studies suggest that CXCL2 is involved in Alzheimer disease, multiple sclerosis and brain ischemia.

参考文献:

1. Vansaun MN. et al. (2013). PLoS One. 8(9):e73054. 2. Jablonska J. et al. (2014). Int J Cancer. 134:1346-58. 3. Oue E. et al. (2012). Biochem Biophys Res Commun. 424:456-461. 4. Haraguchi K. et al. (2012). J. Neurosci.32:3931-3941. 5. L. Bozoyan. et al. (2015). J. Neuroinflammation. 12:173. 6. Hosking MP. et al. (2010). PLoS One. 5(6):e11340.