Lunatic Fringe Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

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产品规格:
  • 50μL
  • 100μL
货号:

FAB2614792

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商品描述
  • 靶点-Target

    Lunatic Fringe

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    42kD

  • 推荐稀释比

    WB 1:500-1:2000;ELISA 1:10000;Not yet tested in other applications.

  • 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

    The antiserum was produced against synthesized peptide derived from human LFNG. AA range:121-170

  • 特异性

    Lunatic Fringe Polyclonal Antibody detects endogenous levels of Lunatic Fringe protein.

  • 基因名称

    LFNG

  • 蛋白名称

    Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe

  • 别名

    LFNG;Beta-1;3-N-acetylglucosaminyltransferase lunatic fringe;O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase

  • Organism-1

    Human

  • 基因ID-1

    3955

  • SwissProt-1

    Q8NES3

  • Organism-2

    Mouse

  • 基因ID-2

    16848

  • SwissProt-2

    O09010

  • Organism-3

    Rat

  • 基因ID-3

    170905

  • SwissProt-3

    Q924T4

  • 背景

    This gene is a member of the fringe gene family which also includes radical and manic fringe genes. They all encode evolutionarily conserved glycosyltransferases that act in the Notch signaling pathway to define boundaries during embryonic development. While their genomic structure is distinct from other glycosyltransferases, fringe proteins have a fucose-specific beta-1,3-N-acetylglucosaminyltransferase activity that leads to elongation of O-linked fucose residues on Notch, which alters Notch signaling. This gene product is predicted to be a single-pass type II Golgi membrane protein but it may also be secreted and proteolytically processed like the related proteins in mouse and Drosophila (PMID: 9187150). Mutations in this gene have been associated with autosomal recessive spondylocostal dysostosis 3. Multiple transcript variants encoding different isoforms

  • 细胞定位

    Golgi apparatus membrane ; Single-pass type II membrane protein .