FGD1 rabbit pAb

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¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2605410

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商品描述
  • 靶点-Target

    FGD1

  • 反应性

    Human,Mouse

  • 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 FGD1 AA range: 508-558

  • 特异性

    This antibody detects endogenous levels of FGD1 at Human/Mouse

  • 基因名称

    FGD1 FGDY ZFYVE3

  • 蛋白名称

    FGD1

  • 别名

    FYVE, RhoGEF and PH domain-containing protein 1;Faciogenital dysplasia 1 protein;Rho/Rac guanine nucleotide exchange factor FGD1;Rho/Rac GEF;Zinc finger FYVE domain-containing protein 3;

  • Organism-1

    Human

  • 基因ID-1

    2245

  • SwissProt-1

    P98174

  • Organism-2

    Mouse

  • 基因ID-2

    14163

  • SwissProt-2

    P52734

  • 背景

    This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of faciogenital dysplasia and X-linked mental retardation, syndromatic 16.[provided by RefSeq, Mar 2011],

  • 细胞定位

    Cytoplasm . Cell projection, lamellipodium . Cell projection, ruffle . Cytoplasm, cytoskeleton . Associated with membrane ruffles and lamellipodia. .