- ￥880
- Bioss
- bs-16005P
- 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-16005P |
| 英文名称 | TLCD3B Antibody Blocking Peptide |
| 中文名称 | FAM57B蛋白封闭多肽 |
| 英文别名 | FA57B_HUMAN; Protein FAM57B. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Membrane. |
| 相似性 | Contains 1 TLC (TRAM/LAG1/CLN8) domain. |
| 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 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The FAM57B gene product has been provisionally designated FAM57B pending further characterization. |
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TLCD3B Antibody Blocking Peptide(bs-16005P)-500ug
￥880
