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SMAD4 抗体

This anti-SMAD4 antibody is a 兔 多克隆 antibody detecting SMAD4 in WB 和 IF. Suitable for 人 和 小鼠.
产品编号 ABIN6989887
发货至: 中国

Quick Overview for SMAD4 抗体 (ABIN6989887)

抗原

See all SMAD4 抗体
SMAD4 (SMAD Family Member 4 (SMAD4))

适用

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  • 3
  • 3
  • 2
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人, 小鼠

宿主

  • 80
  • 22
  • 1
  • 1

克隆类型

  • 62
  • 42
多克隆

标记

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  • 7
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  • 2
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  • 1
  • 1
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This SMAD4 antibody is un-conjugated

应用范围

  • 64
  • 43
  • 36
  • 30
  • 22
  • 13
  • 8
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  • 3
  • 3
  • 3
  • 2
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Western Blotting (WB), Immunofluorescence (IF)
  • 交叉反应

    人, 小鼠

    纯化方法

    Purified by Protein A.

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 160-450 of human SMAD4 (NP_005350.1).

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IF()

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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 for 12 months.

    有效期

    12 months
  • 抗原

    SMAD4 (SMAD Family Member 4 (SMAD4))

    别名

    SMAD4

    背景

    Synonyms: DPC4,JIP,MADH4,MYHRS,Smad4,SMAD4

    Background: This gene encodes a member of the Smad family of signal transduction proteins. Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to TGF-beta signaling. The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins, which then accumulate in the nucleus and regulate the transcription of target genes. This protein binds to DNA and recognizes an 8-bp palindromic sequence (GTCTAGAC) called the Smad-binding element (SBE). The Smad proteins are subject to complex regulation by post-translational modifications. Mutations or deletions in this gene have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome.

    基因ID

    4089

    UniProt

    Q13485

    途径

    Cell Division Cycle, Chromatin Binding, Autophagy
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