- ￥880
- Bioss
- bs-16102P
- 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-16102P |
| 英文名称 | FLJ11506 Antibody Blocking Peptide |
| 中文名称 | AAGAB蛋白封闭多肽 |
| 英文别名 | FLJ11506; AAGAB_HUMAN; Alpha and gamma adaptin binding protein p34; Alpha- and gamma-adaptin-binding protein p34; LOC79719; |
| 纯化方法 | HPLC |
| 研究领域 | Signal Transduction > Protein Trafficking > Vesicle Transport > Regulation |
| 亚基 | Associated with AP-1 and AP-2 complexes. |
| 亚细胞定位 | Cytoplasm, cytosol. |
| 组织特异性 | Widely expressed, including in skin and keratinocytes, with highest levels in adrenal gland, rectum and thymus. |
| 功能 | May play a role in membrane traffic. |
| 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 | Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FLJ11506 gene product has been provisionally designated FLJ11506 pending further characterization. |
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FLJ11506 Antibody Blocking Peptide(bs-16102P)-500ug
￥880
