SHOX2 rabbit pAb

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2617985

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商品描述
  • 靶点-Target

    SHOX2

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,IHC,Flow Cyt

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    36kD

  • 推荐稀释比

    WB 1:500-2000;IHC 1:50-300,Flow Cyt 1:100-200

  • 组成

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • 纯化工艺

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 浓度

    1 mg/ml

  • 克隆性

    Polyclonal

  • 免疫原

    Synthesized peptide derived from human SHOX2 AA range: 37-87

  • 特异性

    This antibody detects endogenous levels of SHOX2 at Human/Mouse/Rat

  • 基因名称

    SHOX2 OG12X SHOT

  • 蛋白名称

    SHOX2

  • Organism-1

    Human

  • 基因ID-1

    6474

  • SwissProt-1

    O60902

  • Organism-2

    Mouse

  • 基因ID-2

    20429

  • SwissProt-2

    P70390

  • Organism-3

    Rat

  • 基因ID-3

    25546

  • SwissProt-3

    O35750

  • 背景

    This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox 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 homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated 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 results in multiple transcript variants. [provided by RefSeq, Jul 2009],

  • 细胞定位

    Nucleus.