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SHOX2 抗体 (Middle Region)

This anti-SHOX2 antibody is a 兔 多克隆 antibody detecting SHOX2 in WB. Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN1109006
发货至: 中国

Quick Overview for SHOX2 抗体 (Middle Region) (ABIN1109006)

抗原

See all SHOX2 抗体
SHOX2 (Short Stature Homeobox 2 (SHOX2))

适用

  • 21
  • 10
  • 8
  • 5
  • 5
  • 5
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  • 3
  • 2
  • 2
  • 2
人, 大鼠, 小鼠

宿主

  • 11
  • 10

克隆类型

  • 14
  • 7
多克隆

标记

  • 18
  • 1
  • 1
  • 1
This SHOX2 antibody is un-conjugated

应用范围

  • 18
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    序列

    SEARVQVWFQ NRRAKCRKQE NQLHKGVLIG AASQFEACRV APYVNVGALR

    交叉反应 (详细)

    Species reactivity (expected):Mouse, RatSpecies reactivity (tested):Human

    纯化方法

    Purified using peptide immunoaffinity column

    免疫原

    The immunogen for anti-SHOX2 antibody: synthetic peptide directed towards the middle region of human SHOX2
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 溶解方式

    Add 50 μL of distilled water to a final concentration of 1 mg/mL.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
  • 抗原

    SHOX2 (Short Stature Homeobox 2 (SHOX2))

    别名

    SHOX2 / SHOT

    背景

    SHOX2 is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients. This gene is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing has been observed at this locus and two variants, each encoding a distinct isoform, have been identified.Synonyms: Homeobox protein Og12X, OG12X, Paired-related homeobox protein SHOT, Short stature homeobox protein 2

    基因ID

    6474

    NCBI登录号

    NP_006875

    途径

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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