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Homeobox D13 抗体 (Middle Region)

This anti-Homeobox D13 antibody is a 兔 多克隆 antibody detecting Homeobox D13 in WB 和 EIA. Suitable for 人 和 小鼠.
产品编号 ABIN952786
发货至: 中国

Quick Overview for Homeobox D13 抗体 (Middle Region) (ABIN952786)

抗原

See all Homeobox D13 (HOXD13) 抗体
Homeobox D13 (HOXD13)

适用

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人, 小鼠

宿主

  • 37
  • 2
  • 1

克隆类型

  • 40
多克隆

标记

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This Homeobox D13 antibody is un-conjugated

应用范围

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Western Blotting (WB), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 7
    • 7
    • 4
    • 4
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    • 2
    • 2
    • 1
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    • 1
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    AA 201-230, Middle Region

    特异性

    This antibody recognizes Human and Mouse HOXD13 / HOX4I (C-term).

    纯化方法

    Protein A column, followed by peptide affinity purification

    免疫原

    KLH conjugated synthetic peptide between 201-230 amino acids from the Central region of human HOXD13 / HOX4I

    亚型

    Ig Fraction
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.25 mg/mL

    缓冲液

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    Homeobox D13 (HOXD13)

    别名

    HOXD13 / HOX4I

    背景

    This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.Synonyms: Homeobox protein Hox-D13, Hox-4I

    分子量

    36101 Da

    基因ID

    3239

    NCBI登录号

    NP_000514

    途径

    Synaptic Membrane
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