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Recombinant SOX17 抗体

The 兔 单克隆 anti-SOX17 antibody (Clone A676) (ABIN7828584) specifically detects SOX17 in WB 和 IHC. The antibody is reactive with 人 samples.
产品编号 ABIN7828584
发货至: 中国
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北京 101111
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Beijing Economic Technological Development Area
Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for Recombinant SOX17 抗体 (ABIN7828584)

抗原

See all SOX17 抗体
SOX17 (SRY (Sex Determining Region Y)-Box 17 (SOX17))

抗体类型

Recombinant Antibody

适用

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宿主

  • 39
  • 11
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克隆类型

  • 42
  • 11
单克隆

标记

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  • 2
  • 1
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This SOX17 antibody is un-conjugated

应用范围

  • 42
  • 14
  • 10
  • 7
  • 3
  • 2
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  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)

克隆位点

A676
  • 原理

    Recombinant SOX17 Monoclonal Antibody

    纯化方法

    Protein A purified

    免疫原

    Recombinant human SOX17 fragment

    亚型

    IgG, kappa
  • 应用备注

    WB 1:1000-1:2000,IHC 1:100-1:200

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

    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 Valid for 12 months. Avoid freeze / thaw cycles.

    有效期

    12 months
  • 抗原

    SOX17 (SRY (Sex Determining Region Y)-Box 17 (SOX17))

    别名

    SOX17

    背景

    VUR,SOX,VUR3,SOX17,SRY-related high mobility group box (SOX) proteins comprise a large family of widely conserved transcription factors. SOX proteins do not directly mediate transcription, but require binding partners that regulate their ability to mediate transcription of target genes that control cell fate determination and development .Transcription factor Sox17 is a Sox family protein with an established role in endoderm specification during development. In addition, Sox17 plays essential roles in the maintenance of the hematopoietic stem cell pool and for vascular morphogenesis during development. Sox17 negatively regulates oligodendrocyte precursor differentiation by antagonizing β-catenin signaling. Mutation in the correspondingSox17gene in humans is associated with a form of vesicoureteral reflux, a disorder characterized by congenital kidney and urinary tract defects. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

    分子量

    Calculated MW: 55 kDa

    Observed MW: 55 kDa

    UniProt

    Q9H6I2
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