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GCM2 抗体 (Center)

This anti-GCM2 antibody is a 兔 多克隆 antibody detecting GCM2 in WB. Suitable for 人.
产品编号 ABIN2856796
发货至: 中国

Quick Overview for GCM2 抗体 (Center) (ABIN2856796)

抗原

See all GCM2 抗体
GCM2 (Glial Cells Missing Homolog 2 (GCM2))

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 GCM2 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    Center

    产品特性

    Rabbit polyclonal antibody to GCM2 (glial cells missing homolog 2 (Drosophila))
    GCM2 antibody [N3C3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the center region of human GCM2. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    Suggested dilution Reference Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceWestern blot1:500-1:3000*

    说明

    Positive Control: A431

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.75 mg/mL

    缓冲液

    0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    GCM2 (Glial Cells Missing Homolog 2 (GCM2))

    别名

    GCM2

    背景

    This gene is a homolog of the Drosophila glial cells missing gene, which is thought to act as a binary switch between neuronal and glial cell determination. The protein encoded by this gene contains a conserved N-terminal GCM motif that has DNA-binding activity. The protein is a transcription factor that acts as a master regulator of parathyroid development. It has been suggested that this transcription factor might mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. Mutations in this gene are associated with hypoparathyroidism.

    Cellular Localization: Nucleus

    分子量

    57 kDa

    基因ID

    9247
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