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MECP2 抗体

This anti-MECP2 antibody is a 兔 多克隆 antibody detecting MECP2 in WB 和 IHC. Suitable for 人 和 小鼠.
产品编号 ABIN6566655
发货至: 中国

Quick Overview for MECP2 抗体 (ABIN6566655)

抗原

See all MECP2 抗体
MECP2 (Methyl CpG Binding Protein 2 (MECP2))

适用

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人, 小鼠

宿主

  • 103
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克隆类型

  • 104
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多克隆

标记

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This MECP2 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 纯化方法

    Affinity purification

    免疫原

    Recombinant protein of human MECP2

    亚型

    IgG
  • 应用备注

    WB 1:500 - 1:1000 IHC 1:50 - 1:100

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    MECP2 (Methyl CpG Binding Protein 2 (MECP2))

    别名

    MECP2

    背景

    Synonyms: AUTSX 3,AUTSX3,DKFZp686A24160,Mbd 5,Mbd5,MECP 2,MeCP 2 protein,MeCP-2 protein,Mecp2,MECP2,Methyl CpG binding protein 2 (Rett syndrome),Methyl CpG binding protein 2,Methyl-CpG-binding protein 2,MRX 16,MRX 79,MRX16,MRX79,MRXS 13,MRXS13,MRXSL,PPMX,RS,RTS,RTT,WBP 10,WBP10

    Background: 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 most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. Alternative splicing results in multiple transcript variants encoding different isoforms.

    分子量

    Observed_MW: 83kDa

    Calculated_MW: 52kDa/53kDa

    基因ID

    4204

    UniProt

    P51608

    途径

    Inositol Metabolic Process, Chromatin Binding, Synaptic Membrane
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