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MEF2A 抗体 (AA 391-497)

This anti-MEF2A antibody is a 小鼠 单克隆 antibody detecting MEF2A in ELISA. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN1724919
发货至: 中国

Quick Overview for MEF2A 抗体 (AA 391-497) (ABIN1724919)

抗原

See all MEF2A 抗体
MEF2A (Myocyte Enhancer Factor 2A (MEF2A))

适用

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宿主

  • 136
  • 6
小鼠

克隆类型

  • 126
  • 16
单克隆

标记

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This MEF2A antibody is un-conjugated

应用范围

  • 94
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ELISA

克隆位点

2F9H2
  • 抗原表位

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    • 1
    AA 391-497

    原理

    MEF2A Antibody

    纯化方法

    Purified antibody

    免疫原

    Purified recombinant fragment of human MEF2A (AA: 391-497) expressed in E. Coli.

    亚型

    IgG1
  • 应用备注

    ELISA: 1/10000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified antibody in PBS with 0.05 % 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

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Zhao, Zhao, Peng: "The effects of myocyte enhancer factor 2A gene on the proliferation, migration and phenotype of vascular smooth muscle cells." in: Cell biochemistry and function, Vol. 30, Issue 2, pp. 108-13, (2012) (PubMed).

    Guella, Rimoldi, Asselta, Ardissino, Francolini, Martinelli, Girelli, Peyvandi, Tubaro, Merlini, Mannucci, Duga: "Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease." in: Circulation. Cardiovascular genetics, Vol. 2, Issue 2, pp. 165-72, (2009) (PubMed).

  • 抗原

    MEF2A (Myocyte Enhancer Factor 2A (MEF2A))

    别名

    MEF2A

    背景

    The protein encoded by this gene is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). Several transcript variants encoding different isoforms have been found for this gene.

    分子量

    54.8 kDa

    UniProt

    Q02078

    途径

    Neurotrophin Signaling Pathway, Activation of Innate immune Response, Carbohydrate Homeostasis, Chromatin Binding, Regulation of Muscle Cell Differentiation, Toll-Like Receptors Cascades
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