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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
Acasunlimab
- 抗体英文名:
Anti-Human PDL1x4-1BB antibody (Acasunlimab Biosimilar )
- 靶点:
CD274 (programmed cell death 1 ligand 1, B7H1, B7-H1, PDL1, PD-L1, PDCD1L1, B7 homolog 1, B7 homologue 1) [Homo sapiens]TNFRSF9 (tumor necrosis factor receptor (TNFR) superfamily member 9, 4-1BB, T cell antigen ILA, CD137) [Homo sapiens]bispecific
- 适应物种:
human
- 保质期:
12 months
- 级别:
Research Grade
- 供应商:
苏州艾洛蒙
- 克隆性:
单克隆
- 保存条件:
Store at -20°C for 12 months (Avoid repeated freezing and thawing)
- 形态:
Liquid
- 亚型:
Human IgG1, κ
- 规格:
1mg
Acasunlimab (GEN1046) 是一种双特异性抗体 (bsAb),靶向PD-L1和4-1BB。Acasunlimab 通过有条件的4-1BB 刺激增强 T 细胞和 NK 细胞功能,同时构成性地阻断PD-1/PD-L1抑制轴。Acasunlimab 可用于癌症的研究。Acasunlimab (GEN1046), a bispecific antibody (bsAb) designed to target PD-L1 and 4-1BB, functions by enhancing both T-cell and NK-cell response via conditional 4-1BB stimulation and continuously inhibiting the PD-1/PD-L1 axis. This compound is applicable in cancer research.
Acasunlimab (DuoBody-PD-L1×4-1BB) is an investigational, bispecific antibody designed to elicit an antitumor immune response via conditional 4-1BB activation strictly dependent on simultaneous programmed death-ligand 1 (PD-L1) binding. Since 4-1BB is coexpressed with programmed cell death protein-1 (PD-1) on CD8+ T cells, PD-1 blockade and simultaneous costimulation through 4-1BB may synergistically enhance T-cell effector functions. We hypothesized that combining acasunlimab with PD-1 blockade to fully disrupt PD-1 interactions with both PD-L1 and PD-L2 would amplify the depth and duration of antitumor immunity.
Acasunlimab(DuoBody-PD-L1×4-1BB)是一种试验用双特异性抗体,设计用于通过严格依赖于同时程序性死亡配体1(PD-L1)结合的条件性4-1BB活化引发抗肿瘤免疫应答。由于4-1BB与CD 8 + T细胞上的程序性细胞死亡蛋白-I(PD-1)共表达,因此PD-1阻断和通过4-1BB的同时共刺激可以协同增强T细胞效应器功能。我们假设,将acasunlimab与PD-1阻断剂联合使用以完全破坏PD-1与PD-L1和PD-L2的相互作用,将扩大抗肿瘤免疫的深度和持续时间。

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文献和实验aberrantly expressed in human cancers detected by autologous antibody screening. Proc. Natl. Acad. Sci. USA, 1997, 94; 1914 6. James W. Hodge, Carcinoembryonic antigen as a target for cancer vaccines. Cancer Immunol Immunother, 1996, 43:127 7. Tuttle T
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