Human Osteoprotegerin / TNFRSF11B Protein-null-试剂-生物在线
北京百普赛斯生物科技股份有限公司
Human Osteoprotegerin / TNFRSF11B Protein

Human Osteoprotegerin / TNFRSF11B Protein

商家询价

产品名称: Human Osteoprotegerin / TNFRSF11B Protein

英文名称: Human Osteoprotegerin / TNFRSF11B Protein

产品编号: TNB-H5220

产品价格: 0

产品产地: USA

品牌商标: ACROBiosystems

更新时间: null

使用范围: null

北京百普赛斯生物科技股份有限公司
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  • 地址 : 北京经济技术开发区宏达北路8号5号楼4层
  • 邮编 : 100176
  • 所在区域 : 北京
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  • 邮箱 : order.cn@acrobiosystems.com

分子量:20.8 kDa

纯度:>95% as determined by SDS-PAGE.

内毒素:Less than 1.0 EU per μg of the Mouse CD40, His Tag by the LAL method.

Buffer:PBS, pH7.4

生物活性:

产品特性:Mouse CD40, His Tag is fused with a polyhistidine tag at the C-terminus, and has a calculated MW of 20.8 kDa. The predicted N-terminus is Val 24. The reducing (R) protein migrates as 30 kDa in SDS-PAGE  due to glycosylation.

产品背景:CD40 is also known as TNFRSF5, Bp50, CDW40, MGC9013, TNFRSF5 and  p50, is a member of the TNF receptor superfamily which are single transmembrane-spanning glycoproteins, and plays an essential role in mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. CD40 is a costimulatory protein found on antigen presenting cells and is required for their activation. The binding of CD154 (CD40L) on TH cells to CD40 activates antigen presenting cells and induces a variety of downstream effects. CD40 contains 4 cysteine-rich repeats in the extracellular domain, and is expressed in B cells, dendritic cells, macrophages, endothelial cells, and several tumor cell lines. The extracellular domain has the cysteinerich repeat regions, which are characteristic for many of the receptors of the TNF superfamily. Interaction of CD40 with its ligand, CD40L, leads to aggregation of CD40 molecules,which in turn interact with cytoplasmic components to initiate signaling pathways. Early studies on the CD40-CD40L system revealed its role in humoral immunity. Defects in CD40 result in hyper-IgM immunodeficiency type 3 (HIGM3), an autosomal recessive disorder characterized by an inability of B cells to undergo isotype switching, as well as an inability to mount an antibody-specific immune response, and a lack of germinal center formation. 
SDS-PAGE