Rilotumumab
CAS No. 872514-65-3
Rilotumumab ( —— )
产品货号. M36702 CAS No. 872514-65-3
Rilotumumab (AMG 102) 是一种 anti-HGF (抗肝细胞生长因子) 的单克隆抗体,抑制 HGF/MET 驱动的信号传导。Rilotumumab 具有抗肿瘤活性,可用于去势抵抗性前列腺癌 (CRPC) 和实体瘤的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥5216 | 有现货 |
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| 10MG | ¥7106 | 有现货 |
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| 25MG | ¥10137 | 有现货 |
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| 50MG | ¥13764 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Rilotumumab
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Rilotumumab (AMG 102) 是一种 anti-HGF (抗肝细胞生长因子) 的单克隆抗体,抑制 HGF/MET 驱动的信号传导。Rilotumumab 具有抗肿瘤活性,可用于去势抵抗性前列腺癌 (CRPC) 和实体瘤的研究。
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产品描述Rilotumumab (AMG 102) is an anti-HGF (anti-hepatocyte growth factor) monoclonal antibody, inhibits HGF/MET-driven signaling. Rilotumumab shows anti-tumor activity, and can be used in castration-resistant prostate cancer (CRPC) and solid tumor research.
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体外实验Rilotumumab (10 μg/mL; overnight) shows the decrease of MET phosphorylation at Y1234 and Y1235, and an increase in total MET.Western Blot Analysis Cell Line:U87MG.vIII cells Concentration:10 μg/mL Incubation Time:Overnight Result:Showed MET phosphorylation at tyrosine residue 1234 (Y1234) and Y1235 ~50% lower in U87MG.vIII cells than in untreated cells.Showed an increase in total MET compared with untreated cells.
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体内实验Rilotumumab (intraperitoneal injection; 1.5 mg/kg; once two days; 11 d) treatment inhibits glioma cell growth in vivo.Animal Model:6-8-week-old BALB/c nu/nu female mice subcutaneous injected with U87MG.vIII cells Dosage:1.5 mg/kg Administration: Intraperitoneal injection; 1.5 mg/kg; once two days; 11 days Result:Reduced U87MG.vIII xenograft growth (P=0.0002) compared with vehicle-treated xenografts (P=0.0001).
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同义词——
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通路Angiogenesis
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靶点c-Met/HGFR
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受体c-Met/HGFR
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研究领域——
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适应症——
化学信息
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CAS Number872514-65-3
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分子量
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分子式——
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纯度>98% (HPLC)
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溶解度——
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SMILES——
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Ryan CJ, et al. Targeted MET inhibition in castration-resistant prostate cancer: a randomized phase II study and biomarker analysis with rilotumumab plus mitoxantrone and prednisone. Clin Cancer Res. 2013 Jan 1;19(1):215-24.?
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