MECP2 抗体 (pSer421)
Quick Overview for MECP2 抗体 (pSer421) (ABIN2794307)
抗原
See all MECP2 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- pSer421
-
原理
- Rabbit Anti-Human Phospho-MeCP2(S421) Antibody
-
免疫原
- This MeCP2 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding S421 of human MeCP2.
-
亚型
- Ig Fraction
-
-
-
-
应用备注
-
Dot Blot
Recommended Dilutions
DB: 1:500
Dot blot analysis of anti-Phospho-MeCP2-S421 Pab on nitrocellulose membrane. 50 ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.5 μg per ml. -
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 0.350 mg/mL
-
储存条件
- 4 °C,-20 °C
-
储存方法
- 2-8°C (short-term), -20°C (long-term)
-
-
- MECP2 (Methyl CpG Binding Protein 2 (MECP2))
-
别名
- MeCP2
-
背景
-
Target Description: 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.
Gene Symbol: MECP2
-
分子量
- 52441 Da
-
基因ID
- 4204
-
UniProt
- P51608
-
途径
- Inositol Metabolic Process, Chromatin Binding, Synaptic Membrane
抗原
-