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别名 莫妥组单抗
Oportuzumab(常以 Oportuzumab monatox 或 Vicineum 形式进行研究)是一种针对上皮细胞粘附分子 (EpCAM/CD326) 的人源化重组融合蛋白。该分子由抗 EpCAM 的单链抗体片段 (scFv) 与经过修饰的铜绿假单胞菌外毒素 A (ETA) 截短片段共价连接而成。EpCAM 在上皮来源的恶性肿瘤(特别是膀胱癌)中高度表达。Oportuzumab 通过特异性结合肿瘤表面的 EpCAM 蛋白,经内吞作用进入细胞,随后外毒素载荷释放到细胞质中。外毒素通过不可逆地抑制真核延伸因子 2 (eEF-2) 来阻断蛋白质合成,最终诱导癌细胞凋亡
Oportuzumab(常以 Oportuzumab monatox 或 Vicineum 形式进行研究)是一种针对上皮细胞粘附分子 (EpCAM/CD326) 的人源化重组融合蛋白。该分子由抗 EpCAM 的单链抗体片段 (scFv) 与经过修饰的铜绿假单胞菌外毒素 A (ETA) 截短片段共价连接而成。EpCAM 在上皮来源的恶性肿瘤(特别是膀胱癌)中高度表达。Oportuzumab 通过特异性结合肿瘤表面的 EpCAM 蛋白,经内吞作用进入细胞,随后外毒素载荷释放到细胞质中。外毒素通过不可逆地抑制真核延伸因子 2 (eEF-2) 来阻断蛋白质合成,最终诱导癌细胞凋亡

| 产品描述 | Oportuzumab (commonly studied as Oportuzumab monatox or Vicineum) is a humanized recombinant fusion protein specifically targeting the epithelial cell adhesion molecule (EpCAM/CD326). It consists of a single-chain variable fragment (scFv) directed against EpCAM covalently linked to a truncated, modified fragment of Pseudomonas exotoxin A (ETA). EpCAM is significantly overexpressed in epithelial-derived malignancies, particularly bladder cancer. Oportuzumab binds specifically to the EpCAM protein on the tumor cell surface and is internalized via endocytosis, after which the toxin payload is released into the cytoplasm. The toxin irreversibly inhibits eukaryotic elongation factor 2 (eEF-2), thereby blocking protein synthesis and ultimately inducing apoptosis in cancer cells. |
| 别名 | 莫妥组单抗 |
| 反应种属 | Human |
| 应用 | ELISA FACS Functional assay |
| 抗体种类 | Monoclonal |
| 缓冲液 | Supplied as a sterile solution in a buffered formulation system (e.g., phosphate-, citrate-, or amino acid-based). Please refer to the CoA for lot-specific composition. |
| 内毒素 | <1.0 EU/mg |
| 同型 | IgG1 |
| 偶联 | Unconjugated |
| Uniprot ID | |
| 靶点 | EpCAM/TROP1/CD326 |
| CAS No. | 945228-48-8 |
| 存储 |
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