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GCM2 抗体 (AA 61-160) (Cy5.5)

This anti-GCM2 antibody (ABIN1706532) is a Rabbit Polyclonal antibody detecting GCM2 in WB, IF (cc), IF (p). Suitable for Human.
产品编号 ABIN1706532
发货至: 中国

Quick Overview for GCM2 抗体 (AA 61-160) (Cy5.5) (ABIN1706532)

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 conjugated to Cy5.5

应用范围

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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

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    AA 61-160

    预测反应

    Human,Mouse,Rat,Dog,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GCM2

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

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

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    GCM2 (Glial Cells Missing Homolog 2 (GCM2))

    别名

    GCM2

    背景

    Synonyms: Chorion-specic transcription factor GCMb, GCM mot protein 2, GCMb, Glial cells missing homolog 2, glial cells missing homolog b, GCM2_HUMAN.

    Background: Glial cells missing homolog 2 (GCM2), also known as Chorion-specific transcription factor GCMb, is a 506 amino acid nuclear protein. GCM2 is a transcription factor that acts as an essential regulator of parathyroid development. GCM2 is also thought to mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. GCM2 contains one N-terminal GCM domain, which has DNA binding activity. Mutations of the gene that encodes GCM2 are associated with hypoparathyroidism, an autosomal recessive condition characterized by hypocalcemia and hyperphosphatemia.

    基因ID

    9247

    UniProt

    O75603
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