- ￥1600 - 4990
- 爱必信(absin)
- abs172213
- 上海
- 2025年07月13日
- ELISA, Flow Cyt, Kinetics (BLI), Kinetics (SPR), Functional assay
- CHO
- -
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
Anti-CD340 Reference Antibody(Disitamab Vedotin)
- 抗体英文名：
Anti-CD340 Reference Antibody(Disitamab Vedotin)
- 靶点：
-
- 浓度：
-
- 应用范围：
ELISA, Flow Cyt, Kinetics (BLI), Kinetics (SPR), Functional assay
- 宿主：
CHO
- 适应物种：
-
- 保质期：
1年
- 抗原来源：
-
- 目录编号：
-
- 级别：
-
- 库存：
现货
- 供应商：
爱必信(上海)生物科技有限公司
- 标记物：
-
- 克隆性：
-
- 保存条件：
Store at -80℃ for one year.
- 形态：
液态
- 亚型：
-
- 免疫原：
-
- 规格：
100ug/1mg
| 规格： | 100ug | 产品价格： | ￥1600.0 |
|---|---|---|---|
| 规格： | 1mg | 产品价格： | ￥4990.0 |
| 概述 | |
| 描述 | 内毒素: <1 EU/mg; 纯度: >95% |
| 别名 | ERBB2; HER2 |
| 宿主 | CHO |
| 应用 | ELISA, Flow Cyt, Kinetics (BLI), Kinetics (SPR), Functional assay |
| 分子量 | 144.52 kDa |
| 性能 | |
| 纯化方法 | Protein A affinity column |
| 类型 | Monoclonal Antibody |
| 同种型 | IgG |
| 储存/保存方法 | Store at -80℃ for one year. |
| 存储溶液 | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 308 |
| 靶标 | |
| 背景说明 | Disitamab vedotin is an ADC consisting of a HER2-directed antibody and Monomethyl auristatin E (MMAE). Disitamab vedotin targets HER2 protein on tumors, recognizes and penetrates cancer cells with high precision, and releases the small molecule cytotoxic drug to kill the cancer cell. The ADC is used for the study of various cancers. |
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文献和实验Purification of Immature CD4+CD8+ Thymocytes by Panning with Anti-CD8 Antibody
Most T lymphocytes of the immune system differentiate within the thymus along the CD4/CD8 developmental pathway by a highly ordered process termed thymic selection ( 1 , 2 ). The maturation status of thymocytes is commonly assessed
Anti-CD22 Onconase: Preparation and Characterization
Antibodies can be conjugated to effector molecules to derive targeted therapeutics with properties such as cell-specific cytotoxicity. The murine anti-CD22 antibody RFB4 linked to a member of the ribonuclease A superfamily, Onconase (Onc
In Vitro Antibody Affinity Maturation Targeting Germline Hotspots
residues are most likely to have a major impact on antibody affinity. Here, we describe procedures for germline hotspot mutagenesis with an emphasis on strategies for randomizing hotspots with PCR and phage display, using as an example the anti-CD
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