- ￥880
- Bioss
- bs-15386P
- 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-15386P |
| 英文名称 | GPR162 Antibody Blocking Peptide |
| 中文名称 | G蛋白偶联受体GPR162蛋白封闭多肽 |
| 英文别名 | A 2; A-2; A2; G protein coupled receptor 162; Gene rich cluster gene A protein; Gene rich cluster, A; Gene-rich cluster gene A protein; GP162; GP162_HUMAN; GPR162; GRCA; Probable G protein coupled receptor 162; Probable G-protein coupled receptor 162. |
| 纯化方法 | HPLC |
| 亚细胞定位 | Cell membrane; Multi-pass membrane protein (By similarity). |
| 相似性 | Belongs to the G-protein coupled receptor 1 family. |
| 功能 | Orphan receptor. |
| 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 | G protein-coupled receptors (GPRs), also known as seven transmembrane receptors, heptahelical receptors or 7TM receptors, comprise a superfamily of proteins that play a role in many different stimulus-response pathways. G protein coupled receptors translate extracellular signals into intracellular signals (G protein activation) and they respond to a variety of signaling molecules, such as hormones and neurotransmitters. GPR162 is a 588 amino acid multi-pass membrane protein that functions as an orphan receptor and belongs to the GPR1 family. Existing as two alternatively spliced isoforms, the gene encoding GPR162 maps to human chromosome 12p13.31. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders. |
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GPR162 Antibody Blocking Peptide(bs-15386P)-500ug
￥880
