- ￥880
- Bioss
- bs-17151P
- 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-17151P |
| 英文名称 | STX17 Antibody Blocking Peptide |
| 中文名称 | 突触17封闭多肽 |
| 英文别名 | FLJ20651; MGC102796; MGC126613; MGC126615; Stx17; STX17_HUMAN; Syntaxin 17; Syntaxin-17. |
| 纯化方法 | HPLC |
| 研究领域 | Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation Signal Transduction > Protein Trafficking > Vesicle Transport > SNAPs & SNAREs |
| 亚细胞定位 | Membrane. Appears to be associated with a membrane compartment, perhaps a subset of the ER such as exit or entrance sites. |
| 相似性 | Belongs to the syntaxin family. Contains 1 t-SNARE coiled-coil homology domain. |
| 功能 | Implicated in vesicle trafficking to lysosomes. Could be involved in processes related to cell division. |
| 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 | Syntaxins, a family of proteins involved in the fusion of synaptic vesicles with the plasma membrane, display broad tissue distribution and contain C-terminal hydrophobic domains that direct them to their respective intracellular compartments. Syntaxin 17, also known as STX17, is a 302 amino acid single-pass type IV membrane protein that contains one t-SNARE coiled-coil homology domain and belongs to the syntaxin family. Thought to localize to the endoplasmic reticulum, Syntaxin 17 plays a role in vesicle trafficking to lysosomes and may be involved in processes related to cell division. The gene encoding Syntaxin 17 maps to human chromosome 9, which houses over 900 genes and comprises nearly 4% of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. |
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STX17 Antibody Blocking Peptide(bs-17151P)-500ug
￥880
