OLIG2 (PTR1315) mouse mAb

活动价:

¥880.00

市场价:¥1280.00

一键复制产品信息
产品规格:
  • 50μL
货号:

FAB2601126

  • 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

    OLIG2

  • 反应性

    Human,Mouse,

  • 应用

    WB,IF,ELISA

  • 宿主物种-Host Species

    Mouse

  • 同种型-Isotype

    IgG

  • 修饰-Modification

    Unmodified

  • MW(Calculated)

    32kD

  • MW(Observed)

    32kD

  • 推荐稀释比

    WB 1:500-2000;IF 1:100-500;ELISA 1:1000-5000

  • 组成

    PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

  • 纯化工艺

    Protein G

  • 储存

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

  • 克隆性

    Monoclonal

  • 克隆号

    PTR1315

  • 免疫原

    Synthesized peptide derived from human protein.AA range:1-100

  • 特异性

    This antibody detects endogenous levels of OLIG2 protein.

  • 基因名称

    olig2

  • 别名

    Basic domain helix loop helix protein class B 1;Basic helix loop helix protein class B 1;BHLHB;bHLHB1;bHLHe19;Class B basic helix loop helix protein 1;Class B basic helix-loop-helix protein 1;class E basic helix loop helix protein 19;Class E basic helix-loop-helix protein 19;Human protein kinase C binding protein RACK17;Olig2;OLIG2_HUMAN;Oligo2;Oligodendrocyte lineage transcription factor 2;Oligodendrocyte specific bHLH transcription factor 2;Oligodendrocyte transcription factor 2;OTTHUMP00000067569;OTTHUMP00000067570;PRKCBP2;Protein kinase C binding protein 2;Protein kinase C binding protein RACK17;Protein kinase C-binding protein 2;Protein kinase C-binding protein RACK17;RACK17.

  • Organism-1

    Human

  • 基因ID-1

    10215

  • SwissProt-1

    Q13516

  • Organism-2

    Mouse

  • SwissProt-2

    Q9EQW6

  • 背景

    This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq, Jul 2008],

  • 细胞定位

    Nuclear