SMAL1 rabbit pAb

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2605384

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商品描述
  • 靶点-Target

    SMAL1

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    105kD

  • 推荐稀释比

    WB 1:500-2000

  • 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 SMAL1 AA range: 485-535

  • 特异性

    This antibody detects endogenous levels of SMAL1 at Human/Mouse/Rat

  • 基因名称

    SMARCAL1 HARP

  • 蛋白名称

    SMAL1

  • 别名

    SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1;HepA-related protein;hHARP;Sucrose nonfermenting protein 2-like 1;

  • Organism-1

    Human

  • 基因ID-1

    50485

  • SwissProt-1

    Q9NZC9

  • Organism-2

    Mouse

  • 基因ID-2

    54380

  • SwissProt-2

    Q8BJL0

  • Organism-3

    Rat

  • 基因ID-3

    316477

  • SwissProt-3

    B4F769

  • 背景

    The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency. [provided by RefSeq, Jul 2008],

  • 细胞定位

    Nucleus . Recruited to damaged DNA regions.