货号:A1174814
同义名:
Trastuzumab单抗
/ Anti-Human HER2, Humanized Antibody
Trastuzumab是一种人源化IgG1单克隆抗体,通过与HER2受体结合来阻止其与配体结合。Trastuzumab具有用于HER2阳性乳腺癌和胃癌研究的潜力。


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| 产品名称 | HER2 ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Poziotinib |
++++
HER2, IC50: 5.3 nM |
98% | |||||||||||||||||
| Tyrphostin AG 879 |
+
HER2-Neu, IC50: 1.0 μM |
95% | |||||||||||||||||
| TAK-285 |
+
HER2, IC50: 17 nM |
99%+ | |||||||||||||||||
| ARRY-380 analog | ✔ | 99% | |||||||||||||||||
| Canertinib |
+++
ErbB2, IC50: 9.0 nM |
EGFR | 99%+ | ||||||||||||||||
| (E/Z)-CP-724714 |
++
HER2/ErbB2, IC50: 10 nM |
95% | |||||||||||||||||
| Lapatinib |
+++
ErbB2, IC50: 9.2 nM |
EGFR | 98% | ||||||||||||||||
| AEE788 |
++++
HER2/ErbB2, IC50: 6 nM |
EGFR | 98+% | ||||||||||||||||
| Neratinib |
+
HER2, IC50: 59 nM |
EGFR,Src | 98% | ||||||||||||||||
| BMS-599626 |
+
HER2, IC50: 30 nM |
98% | |||||||||||||||||
| Mubritinib |
++++
HER2/ErbB2, IC50: 6.0 nM |
99%+ | |||||||||||||||||
| Tucatinib |
+++
ErbB2, IC50: 8 nM |
98% | |||||||||||||||||
| Sapitinib |
++++
ErbB2, IC50: 3 nM |
EGFR | 99%+ | ||||||||||||||||
| CUDC-101 |
++
HER2, IC50: 15.7 nM |
EGFR,HDAC | 99%+ | ||||||||||||||||
| Afatinib dimaleate |
++
HER2, IC50: 14 nM |
98% | |||||||||||||||||
| Afatinib |
++
HER2, IC50: 14 nM |
99% | |||||||||||||||||
| Pertuzumab | ✔ | 95% | |||||||||||||||||
| Trastuzumab | ✔ | 99% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 靶点 |
|
| 蛋白种属 | Human |
| 交叉反应性 | Human |
| Isotype | IgG1-Kappa |
| 内毒素 | < 0.001EU/μg, determined by LAL method. |
| 纯化方法 | Purified, Protein A, affinity column |
| 稀释缓冲液 | Sterile PBS or 0.9% saline for reconstitution/dilution. It is recommended to use the reconstituted/diluted product within one month. |
| Concentration | Treated Time | Description | References | |
| H9c2 rat cardiomyocytes | 0, 0.2, 0.5, 1, 10 µM | 12, 24, 48 hours | To investigate the effects of trastuzumab on H9c2 cell viability and oxidative stress. Results showed that trastuzumab reduced H9c2 cell viability and increased intracellular and mitochondrial ROS levels in a dose- and time-dependent manner. | Int J Mol Med. 2022 Feb;49(2):17 |
| JIMT-1 | 0, 1, 2, 5, 10, 20, 50, 100 μg/mL | 72 hours | Evaluate the effect of trastuzumab on the viability of JIMT-1 cells | Mol Cancer. 2023 Jan 10;22(1):6 |
| SKBR3 | 0, 0.5, 1, 2, 5, 10, 20, 40 μg/mL | 72 hours | Evaluate the effect of trastuzumab on the viability of SKBR3 cells | Mol Cancer. 2023 Jan 10;22(1):6 |
| DD282 | 0.1 µM | 72 hours | Testing the effect of trastuzumab on DD282 cells with HER2 variant of unknown significance, resulting in a viability decrease to 85.6%. | Gut. 2019 Feb;68(2):207-217 |
| DD109 | 0.1 µM | 72 hours | Testing the effect of trastuzumab on DD109 cells with HER2 amplification, resulting in a viability decrease to 79.2%. | Gut. 2019 Feb;68(2):207-217 |
| DD107 | 0.1 µM | 72 hours | Testing the effect of trastuzumab on DD107 cells with HER2 activating mutation, resulting in a viability decrease to 70.6%. | Gut. 2019 Feb;68(2):207-217 |
| SNU216 | 10 μg/mL | 48 hours | To evaluate the effect of trastuzumab on the proliferation of SNU216 cells. The results showed that trastuzumab or GLS1 inhibitors alone did not significantly affect the proliferation of trastuzumab-resistant cells, while the combination of BPTES or CB839 with trastuzumab partially inhibited the proliferation of trastuzumab-resistant cells. | Cancer Commun (Lond). 2023 Aug;43(8):909-937. |
| NCI-N87 | 10 μg/mL | 48 hours | To evaluate the effect of trastuzumab on the proliferation of NCI-N87 cells. The results showed that trastuzumab or GLS1 inhibitors alone did not significantly affect the proliferation of trastuzumab-resistant cells, while the combination of BPTES or CB839 with trastuzumab partially inhibited the proliferation of trastuzumab-resistant cells. | Cancer Commun (Lond). 2023 Aug;43(8):909-937. |
| Administration | Dosage | Frequency | Description | References | ||
| Nude mice | HER2-positive breast cancer xenograft model | Intraperitoneal injection | 10 mg/kg | Every 5 days for 4 times | Evaluate the effect of trastuzumab on the growth of HER2-positive breast cancer xenografts | Mol Cancer. 2023 Jan 10;22(1):6 |
| Nude mice | NCI-N87/luc tumor xenograft model | Intraperitoneal | Trastuzumab (10 mg/kg), TFBG (50 mg/kg) | Trastuzumab twice weekly for 3 weeks; TFBG daily for 21 days | To evaluate the efficacy of TFBG combined with trastuzumab in HER2-positive gastric cancer. Results showed that combination therapy significantly inhibited tumor growth and induced tumor regression. | Nat Commun. 2021 May 14;12(1):2812 |
| CAS号 | 180288-69-1 |
| 分子量 | 145.42 kDa |
| SMILES Code | NONE |
| MDL No. | MFCD03702625 |
| 别名 | Trastuzumab单抗 ;Anti-Human HER2, Humanized Antibody |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C:3-6个月-80°C:24个月 |
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