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- Bioss
- bs-22099P
- 2025年10月16日
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500ug
| 产品编号 | bs-22099P |
| 英文名称 | MeCP2 Antibody Blocking Peptide |
| 中文名称 | 甲基化CpG结合蛋白2封闭多肽 |
| 英文别名 | AUTSX 3; AUTSX3; Mbd 5; MECP-2; MeCP 2 protein; Methyl CpG binding protein 2 (Rett syndrome); Methyl CpG binding protein 2; MRX 16; MRX 79; MRX16; MRX79; MRXS 13; MRXS13; MRXSL; PPMX; RTS; RTT; WBP 10; WBP10. MECP2_HUMAN |
| 纯化方法 | HPLC |
| 研究领域 | Epigenetics and Nuclear Signaling > DNA methylation > Methylated DNA Binding Neuroscience > Neurology process > Neurodegenerative disease |
| 亚基 | Interacts with FNBP3 (By similarity). Interacts with CDKL5 |
| 亚细胞定位 | Nucleus. Note=Colocalized with methyl-CpG in the genome. |
| 组织特异性 | Present in all adult somatic tissues tested. |
| 翻译后修饰 | Phosphorylated on Ser-423 in brain upon synaptic activity, which attenuates its repressor activity and seems to regulate dendritic growth and spine maturation |
| 相似性 | Contains 2 A.T hook DNA-binding domains. Contains 1 MBD (methyl-CpG-binding) domain. |
| 功能 | Chromosomal protein that binds to methylated DNA. It can bind specifically to a single methyl-CpG pair. It is not influenced by sequences flanking the methyl-CpGs. Mediates transcriptional repression through interaction with histone deacetylase and the corepressor SIN3A. |
| 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 | DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3 and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of some cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. |
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MeCP2 Antibody Blocking Peptide(bs-22099P)-500ug
￥880
