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MEF2D antibody (AA 431-521)

This anti-MEF2D antibody is a Rabbit Polyclonal antibody detecting MEF2D in WB. Suitable for Human.
Catalog No. ABIN7268733

Quick Overview for MEF2D antibody (AA 431-521) (ABIN7268733)

Target

See all MEF2D Antibodies
MEF2D (Myocyte Enhancer Factor 2D (MEF2D))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This MEF2D antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

    • 19
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    AA 431-521

    Purpose

    MEF2D Rabbit pAb

    Sequence

    TTHPHISIKS EPVSPSRERS PAPPPPAVFP AARPEPGDGL SSPAGGSYET GDRDDGRGDF GPTLGLLRPA PEPEAEGSAV KRMRLDTWTL K

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 431-521 of human MEF2D (NP_005911.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

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

    MEF2D (Myocyte Enhancer Factor 2D (MEF2D))

    Alternative Name

    MEF2D

    Background

    This gene is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Members of this family are involved in control of muscle and neuronal cell differentiation and development, and are regulated by class II histone deacetylases. Fusions of the encoded protein with Deleted in Azoospermia-Associated Protein 1 (DAZAP1) due to a translocation have been found in an acute lymphoblastic leukemia cell line, suggesting a role in leukemogenesis. The encoded protein may also be involved in Parkinson disease and myotonic dystrophy. Alternative splicing results in multiple transcript variants.,MEF2D,Epigenetics & Nuclear Signaling,Transcription Factors,Signal Transduction,ErbB-HER Signaling Pathway,MAPK-P38 Signaling Pathway,Endocrine & Metabolism,AMPK Signaling Pathway,Neuroscience,Cardiovascular,Heart,Cardiogenesis,Hypertrophy,MEF2D

    Molecular Weight

    49kDa/50kDa/55kDa/56kDa

    Gene ID

    4209

    UniProt

    Q14814
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