Product Details
Product Details
Product Specification
| Host | Rat |
| Antigen | IL-6R |
| Synonyms | Interleukin-6 receptor subunit alpha; IL-6 receptor subunit alpha; IL-6R subunit alpha; IL-6R-alpha; IL-6RAAlternative nameIL-6R 1; CD126; Il6r; Il6ra |
| Location | Secreted, Cell membrane |
| Accession | P22272 |
| Clone Number | 15A7 |
| Antibody Type | Rat mAb |
| Isotype | Rat IgG2b, κ |
| Isotype Control | Invivo rat IgG2b isotype control, anti-keyhole limpet hemocyanin |
| Application | in vivo blocking, in vitro blocking |
| Reactivity | Ms |
| Purification | Protein G |
| Concentration | 5 mg/ml |
| Purity | >95% (Determined by SDS-PAGE) |
| Endotoxin | <1EU/mg |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS pH7.4, containing no preservative |
| Stability & Storage | 2 to 8 °C for 2 weeks under sterile conditions; |
Background
The Interleukin-6 receptor (IL-6R) is a critical component of the immune signaling pathway, functioning as either a membrane-bound protein on specific cell surfaces or as a soluble form circulating in the blood, and it plays a pivotal role in mediating the biological effects of interleukin-6 (IL-6), a pleiotropic cytokine involved in acute phase responses, inflammation, hematopoiesis, and immune regulation. Structurally, IL-6R consists of an extracellular domain that binds IL-6, a transmembrane region, and a cytoplasmic tail that lacks intrinsic kinase activity but associates with the signal-transducing subunit gp130; upon IL-6 binding to IL-6R, the complex recruits gp130, leading to its dimerization and the activation of downstream signaling cascades, primarily the JAK/STAT pathway, particularly JAK1/2 and STAT3, which subsequently regulate gene expression related to cell proliferation, differentiation, and survival. This receptor system is essential for both classical signaling, where membrane-bound IL-6R restricts IL-6 activity to cells expressing the receptor, and trans-signaling, where soluble IL-6R allows IL-6 to affect a broader range of cell types lacking membrane-bound IL-6R, thereby amplifying inflammatory responses and contributing to various pathological conditions such as chronic inflammatory diseases, autoimmune disorders, and cancer, making IL-6R a significant therapeutic target for drugs like tocilizumab, which blocks IL-6R to mitigate excessive inflammation.
