021-51111890
购物车（）
sales@molnova.cn
Lexatumumab
CAS No. 845816-02-6
Lexatumumab ( —— )
产品货号. M36731 CAS No. 845816-02-6
Lexatumumab (HGS-ETR 2) 是一种人源激动 TRAIL 受体 2 (TRAIL-R2, DR5, APO-2) IgG4κ 型单克隆抗体。Lexatumumab 在恶性间皮瘤中诱导细胞凋亡 (apoptosis)。Lexatumumab 可用于恶性胸膜间皮瘤 (MPM) 研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ￥3191 | 有现货 |
|
| 5MG | ￥5225 | 有现货 |
|
| 10MG | ￥7970 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Lexatumumab
-
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
-
产品简述Lexatumumab (HGS-ETR 2) 是一种人源激动 TRAIL 受体 2 (TRAIL-R2, DR5, APO-2) IgG4κ 型单克隆抗体。Lexatumumab 在恶性间皮瘤中诱导细胞凋亡 (apoptosis)。Lexatumumab 可用于恶性胸膜间皮瘤 (MPM) 研究。
-
产品描述Lexatumumab (HGS-ETR 2) is a human agonistic TRAIL receptor 2 (TRAIL-R2, DR5, APO-2) IgG4κ type monoclonal antibody. Lexatumumab induces apoptosis in malignant mesothelioma. Lexatumumab can be used for malignant pleural mesothelioma (MPM) research.
-
体外实验Cell Viability Assay Cell Line:Melanoma cell lines Concentration:0.01, 0.1, 1.0 and 10.0 μg/ml Incubation Time:72 h Result:Induced various degrees of cell death in the different cell lines.
-
体内实验Animal Model:FEMX-1 xenografts miceDosage:10 mg/kg, 10 mg/kg+Dacarbazine (62.5 mg/kg once a week, i.p. injection)Administration:i.v., twice a week Result:Increased antitumor effect in vivo when combined with Dacarbazine (HY-B0078). Induced cleavage of livin into its truncated, proapoptotic form, a compound previously shown to accelerate apoptosis.
-
同义词——
-
通路Apoptosis
-
靶点Apoptosis
-
受体Apoptosis
-
研究领域——
-
适应症——
化学信息
-
CAS Number845816-02-6
-
分子量143.6 (kDa)
-
分子式——
-
纯度>98% (HPLC)
-
溶解度——
-
SMILES——
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
-
Imexon
一种 2-氰基氮丙啶衍生物，对某些类型的癌症具有抗肿瘤活性。
-
Exisulind
Exisulind 通过激活蛋白激酶 G (PKG) 诱导细胞凋亡。 Exisulind 在实体瘤和血液癌细胞系中表现出抗肿瘤活性，并且是结肠癌、前列腺癌、膀胱癌、乳腺癌和肺癌啮齿动物模型中肿瘤生长的抑制剂。
-
Cholesteryl Hemisucc...
Cholesteryl Hemisuccinate Tris Salt is an acidic cholesteryl ester with hepatoprotective and anticancer activity.Cholesteryl hemisuccinate is a membrane stabilizer in dipalmitoylphosphatidylcholine liposomes containing Chaikosaponin-d, which enhances the anticancer efficacy of cisplatin.Cholesteryl hemisuccinate possesses antitumor activity, inhibits tumor Cholesteryl hemisuccinate has antitumor activity, inhibits tumor growth, inhibits the hepatotoxicity of acetaminophen (AAP) and prevents AAP-induced apoptosis of hepatocytes.Cholesteryl hemisuccinate protects rodents against the toxic effects of acetaminophen, adriamycin, carbon tetrachloride, chloroform, and galactosamine.
