- ￥880
- Bioss
- bs-8726P
- 2025年10月16日
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- 详细信息
- 技术资料
- 规格：
500ug
| 产品编号 | bs-8726P |
| 英文名称 | BZW2 Antibody Blocking Peptide |
| 中文名称 | BZW2蛋白封闭多肽 |
| 英文别名 | HSPC028; MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2; Basic leucine zipper and W2 domains 2; BZW 2; MST017; BZW2_HUMAN. |
| 纯化方法 | HPLC |
| 研究领域 | Cell Biology > Cell Cycle > Cell differentiation Developmental Biology > Organogenesis > Nervous system development Neuroscience > Neurology process > Neurogenesis |
| 相似性 | Belongs to the BZW family. Contains 1 W2 domain. |
| 功能 | BZW2 belongs to the BZW family and contains one W2 domain. It may be involved in neuronal differentiation. |
| 保存条件 | Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles. |
| 注意事项 | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 背景资料 | BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5% of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia. |
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BZW2 Antibody Blocking Peptide(bs-8726P)-500ug
￥880
