- ￥880
- Bioss
- bs-16022P
- 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-16022P |
| 英文名称 | FAM96A Antibody Blocking Peptide |
| 中文名称 | FAM96A蛋白封闭多肽 |
| 英文别名 | Family with sequence similarity 96, member A; FA96A_HUMAN; FLJ22875. |
| 纯化方法 | HPLC |
| 相似性 | FAM96A belongs to the UPF0195 family. |
| 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 FAM96A gene product has been provisionally designated FAM96A pending further characterization. |
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FAM96A Antibody Blocking Peptide(bs-16022P)-500ug
￥880
