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MECP2 antibody (pSer421)

The Rabbit Polyclonal anti-MECP2 antibody has been validated for DB. It is suitable to detect MECP2 in samples from Human.
Catalog No. ABIN2794307

Quick Overview for MECP2 antibody (pSer421) (ABIN2794307)

Target

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

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This MECP2 antibody is un-conjugated

Application

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Dot Blot (DB)
  • Binding Specificity

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    pSer421

    Purpose

    Rabbit Anti-Human Phospho-MeCP2(S421) Antibody

    Immunogen

    This MeCP2 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding S421 of human MeCP2.

    Isotype

    Ig Fraction
  • Application Notes

    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.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.350 mg/mL

    Storage

    4 °C,-20 °C

    Storage Comment

    2-8°C (short-term), -20°C (long-term)
  • Target

    MECP2 (Methyl CpG Binding Protein 2 (MECP2))

    Alternative Name

    MeCP2

    Background

    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

    Molecular Weight

    52441 Da

    Gene ID

    4204

    UniProt

    P51608

    Pathways

    Inositol Metabolic Process, Chromatin Binding, Synaptic Membrane
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