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MECP2 抗体 (pSer80)

This anti-MECP2 antibody is a 兔 多克隆 antibody detecting MECP2 in ELISA 和 DB. Suitable for 人.
产品编号 ABIN3031767
发货至: 中国

Quick Overview for MECP2 抗体 (pSer80) (ABIN3031767)

抗原

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

适用

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宿主

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克隆类型

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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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ELISA, Dot Blot (DB)
  • 抗原表位

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    pSer80

    交叉反应 (详细)

    Expected species reactivity: Mouse, Rat, Primate

    纯化方法

    Antigen affinity purified

    免疫原

    This phospho-MeCP2 antibody was produced from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding pS80 of human MeCP2.

    亚型

    Ig Fraction
  • 应用备注

    Titration of the phospho-MeCP2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Dot blot: 1:500

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    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

    Aliquot the phospho-MeCP2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    MECP2 (Methyl CpG Binding Protein 2 (MECP2))

    别名

    MeCP2

    背景

    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.

    UniProt

    P51608

    途径

    Inositol Metabolic Process, Chromatin Binding, Synaptic Membrane
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