Peroxin 3 Polyclonal Antibody

活动价:

¥680.00

市场价:¥880.00

一键复制产品信息
产品规格:
  • 50μL
  • 100μL
货号:

FAB2615695

  • 产品信息
  • 注意事项
  • 实验验证
  • 产品声明
  • 引用文献
  • 相关产品
  • 文件下载
商品描述
  • 靶点-Target

    Peroxin 3

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,ELISA,IHC

  • 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 1:500-2000;IHC 1:50-300;ELISA 1:2000-20000

  • 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 PEX3. AA range:12-61

  • 特异性

    Peroxin 3 Polyclonal Antibody detects endogenous levels of Peroxin 3 protein.

  • 基因名称

    PEX3

  • 蛋白名称

    Peroxisomal biogenesis factor 3

  • 别名

    PEX3;Peroxisomal biogenesis factor 3;Peroxin-3;Peroxisomal assembly protein PEX3

  • Organism-1

    Human

  • 基因ID-1

    8504

  • SwissProt-1

    P56589

  • Organism-2

    Mouse

  • 基因ID-2

    56535

  • SwissProt-2

    Q9QXY9

  • Organism-3

    Rat

  • 基因ID-3

    83519

  • SwissProt-3

    Q9JJK4

  • 背景

    The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS). [provided by RefSeq, Oct 20

  • 细胞定位

    Peroxisome membrane ; Multi-pass membrane protein .