- 询价
- DIMA BIOTECH/缔码生物
- 武汉
- CEL100030
- 2025年07月09日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
In Stock
- 供应商：
缔码生物（武汉）科技有限公司
- 是否是肿瘤细胞：
否
- 运输方式：
干冰
- 规格：
5x10^6 Cells/mL
| 产品分类 | Overexpression Stable Cell Line |
|---|---|
| 背景 | This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy. |
| 描述 | Monoclonal Cell Line Derived from K562 Cells, Engineered for Stable Expression of Human TROP2 Using Lentiviral Technology |
| 培养基 | RPMI-1640+10% FBS+1% P.S+1% Gln+2 ug/mL Puromycin |
| 宿主细胞 | K562 |
| 保存及运输 | Cells are shipped using dry ice and require liquid nitrogen storage for long term preservation. |
| 建议对照 | SKU: BME100023 |
| 别名 | TACSTD2; GA733-1; M1S1; TROP2 |
| 声明 | 1. Please inspect cells upon receipt and report any issues promptly. 2. We offer one-time replacements for issues reported within a week of receipt. 3. User-induced issues are not eligible for free replacements. 4. We do not accept liability for damages resulting from cell use, storage, or loss. 5. Feedback received more than one month after receipt will not be processed. |
| 应用 | FACS Data |
| 靶点 | Trop2 |
| uniprot-id | P09758 |
| 用途 | For research use only. |
Figure 1. Flow cytometry analysis of human TROP2 overexpression using Hu_TROP2 K562 Cell Line (Cat. No. CEL100030) and Anti-Trop2 (sacituzumab biosimilar) mAb (Cat. No. BME100023)
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文献和实验指从某初代培养开始通过连续培养所产生的所有细胞。包括从初代培养的细胞和细胞群所发展的一系列的细胞。如果培养的状态清楚，则在前面冠以有限继代性（ finite）或连续继代性（ continuous）。例如，人二倍体成纤细胞系属于前者， HeLa细胞系属后者。另外连续继代性细胞系也称为树立细胞系。
Cell Assessment by At-line Microscopy
and at-line cell monitoring in bioreactors (Akin et al., Biosens Bioelectron 26:4532–4537, 2011; Babitzky et al., At-line microscopic analysis of suspension cell cultures. In: ECCE/ECAB, the first joint European Congress of chemical engineering and applied
A method is described to establish mouse embryonic stem cell (ESC) lines from hybrid and inbred strains of mice. Attention is paid not only to the methodology for isolation and culture but also to the validation of freshly derived lines, in order
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