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Tocilizumab (Anti-Human IL6R) 是抗人白细胞介素-6 受体 (IL-6R) 的中和抗体,能够阻碍 IL-6 与 IL-6R 的结合,进而抑制经典和反式信号。可用于研究类风湿性关节炎,并且被建议作为治疗重症 COVID-19 的可能药物。
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Tocilizumab (Anti-Human IL6R) 是抗人白细胞介素-6 受体 (IL-6R) 的中和抗体,能够阻碍 IL-6 与 IL-6R 的结合,进而抑制经典和反式信号。可用于研究类风湿性关节炎,并且被建议作为治疗重症 COVID-19 的可能药物。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 1,580 | In stock | |
2 mg | ¥ 2,330 | In stock | |
5 mg | ¥ 3,980 | In stock | |
10 mg | ¥ 5,680 | In stock | |
25 mg | ¥ 8,720 | In stock | |
50 mg | ¥ 11,700 | In stock | |
100 mg | ¥ 15,800 | 5日内发货 |
Tocilizumab 相关产品
产品描述 | Tocilizumab (Anti-Human IL6R) is a neutralizing antibody against human interleukin-6 receptor (IL-6R) that blocks the binding of IL-6 to IL-6R, thereby inhibiting both classical and trans signaling. It can be used to study rheumatoid arthritis and has been suggested as a possible drug for the treatment of severe COVID-19. |
体外活性 | 方法:Tocilizumab (Anti-Human IL6R)(0.001–10,000 μg/ml) 培养 Ba/F3-gp130-hIL-6R 或 Ba/F3-gp130-mIL-6R 细胞 2 天,观察细胞增殖情况。 |
体内活性 | 方法:将HARA-B细胞接种到裸鼠心脏的左心室,接种三周后,在接下来的三周内每周静脉注射Tocilizumab (Anti-Human IL6R)(1.0 mg/100 μL,两周一次,三周) 。 |
细胞实验 | Objective: To validate that IL-6 signaling is essential for TAM (tumor-associated macrophages)-enhanced CSC (cancer stem cells) function. Concentrations: 5 μg/ml. Incubation Time: 72 h. Method: For co-culture experiments, 12-well Transwell chambers were used with 2×105 HepG2 or Hep3B cells seeded in the lower chamber one day before co-culture and either 5×105 or 1×106 TAMs added in the upper chamber. Tocilizumab or human IgG antibody were added in indicated experiments to selected wells. After 24 to 72 hours, HCC cells and CD14+ TAM cells were collected separately for analysis. Cells:HepG2 cell lines, TAMs isolated from HCCs (hepatocellular carcinoma) |
别名 | 托珠单抗 |
分子量 | 148 kDa |
CAS No. | 375823-41-9 |
密度 | no data available |
存储 | store at low temperature | -20°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
案例一:设置对照组、IL-6组、IL-6+Tocilizumab组处理HBMEC细胞,通过Western Blot检测紧密连接蛋白(ZO-1、Occludin、Claudin-5)的表达水平。结果发现,IL-6能降低ZO-1、Occludin、Claudin-5的蛋白表达,而cilizumab能逆转IL-6的作用。
引用文献:Meng H, Fan L, Zhang C J, et al. Synthetic VSMCs Induce BBB Disruption Mediated by MYPT1 in Ischemic Stroke. iScience. 2021: 103047.
案例二:将从ScxGFP小鼠中分离的成纤维细胞群,在加或不加Tocilizumab的条件下培养;以及IL-6 KO外植体,在加或不加重组IL-6的条件下培养7天。检测到Tocilizumab处理后总细胞数和ScxGFP+成纤维细胞数都减少,核心区域的ScxGFP+细胞比例下降。添加重组IL-6可部分恢复细胞增殖,但无法完全恢复迁移能力。
引用文献:Stauber T, Moschini G, Hussien A A, et al.Il-6 signaling exacerbates hallmarks of chronic tendon disease by stimulating reparative fibroblasts.eLife.2024, 12.
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