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MLXIPL 抗体

The 兔 多克隆 anti-MLXIPL antibody (ABIN6571243) specifically detects MLXIPL in WB. The antibody is reactive with 人, 大鼠 和 小鼠 samples.
产品编号 ABIN6571243
发货至: 中国
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Quick Overview for MLXIPL 抗体 (ABIN6571243)

抗原

See all MLXIPL 抗体
MLXIPL (MLX Interacting Protein-Like (MLXIPL))

适用

  • 37
  • 24
  • 12
  • 5
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 49
  • 3

克隆类型

  • 49
  • 3
多克隆

标记

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  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This MLXIPL antibody is un-conjugated

应用范围

  • 26
  • 15
  • 14
  • 13
  • 13
  • 10
  • 9
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 纯化方法

    Affinity purification

    免疫原

    Recombinant protein of human MLXIPL

    亚型

    IgG
  • 应用备注

    WB 1:500 - 1:2000

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    MLXIPL (MLX Interacting Protein-Like (MLXIPL))

    别名

    MLXIPL

    背景

    Synonyms: carbohydrate response element binding protein,bHLHd14,Carbohydrate responsive element binding protein,Class D basic helix-loop-helix protein 14,MIO,MLX interacting protein like,Mlx interactor,MLX-interacting protein-like,MLXIPL,MONDOB,WBS14,WBSCR 14,WBSCR14,Williams Beuren syndrome chromosome region 14,Williams Beuren syndrome chromosome region 14 protein,Williams-Beuren syndrome chromosomal region 14 protein,WS basic helix loop helix leucine zipper protein,WS basic-helix-loop-helix leucine zipper protein,WS bHLH,WS-bHLH

    Background: This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants.

    分子量

    Observed_MW: 93kDa

    Calculated_MW: 62kDa/78kDa/90kDa/92kDa/93kDa

    基因ID

    51085

    UniProt

    Q9NP71

    途径

    Carbohydrate Homeostasis, Regulation of Carbohydrate Metabolic Process
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