Fibulin-5 Monoclonal Antibody

活动价:

¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2600633

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商品描述
  • 靶点-Target

    Fibulin-5

  • 反应性

    Human

  • 应用

    WB,IHC,IF,ELISA

  • 宿主物种-Host Species

    Mouse

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    50kD

  • 推荐稀释比

    WB 1:500-1:2000;IHC 1:200-1:1000;ELISA 1:10000;IF 1:50-200

  • 组成

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

  • 纯化工艺

    Affinity purification

  • 储存

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

  • 克隆性

    Monoclonal

  • 免疫原

    Purified recombinant fragment of Fibulin-5 expressed in E. Coli.

  • 特异性

    Fibulin-5 Monoclonal Antibody detects endogenous levels of Fibulin-5 protein.

  • 基因名称

    FBLN5

  • 蛋白名称

    Fibulin-5

  • 别名

    FBLN5;DANCE;Fibulin-5;FIBL-5;Developmental arteries and neural crest EGF-like protein;Dance;Urine p50 protein;UP50

  • Organism-1

    Human

  • 基因ID-1

    10516

  • SwissProt-1

    Q9UBX5

  • Organism-2

    Mouse

  • SwissProt-2

    Q9WVH9

  • 背景

    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq, Jul 2008],

  • 细胞定位

    Secreted . Secreted, extracellular space, extracellular matrix . co-localizes with ELN in elastic fibers. .