- ￥880
- Bioss
- bs-12165P
- 2026年10月10日
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- 技术资料
- 规格：
500ug
| 产品编号 | bs-12165P |
| 英文名称 | ESYT3 Antibody Blocking Peptide |
| 中文名称 | 延伸突触蛋白3封闭多肽 |
| 英文别名 | CHR3SYT; E Syt3; ESYT3; Extended synaptotagmin 3; Extended synaptotagmin-like protein 3; ESYT3_HUMAN. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Cell membrane; Single-pass membrane protein. |
| 组织特异性 | Widely expressed with high level in cerebellum and skin. _x000D_ |
| 相似性 | Belongs to the extended synaptotagmin family._x000D_
Contains 3 C2 domains. _x000D_ |
| 功能 | FAM62C belongs to the extended synaptotagmin family. It is a single-pass membrane protein, and contains 3 C2 domains. FAM62C may play a role as calcium-regulated intrinsic membrane protein. |
| 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 | Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. The FAM62C gene product has been provisionally designated FAM62C pending further characterization. |
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ESYT3 | FAM62C Ab Blocking Peptide(bs-12165P)-500ug
￥880
