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您当前的位置:首页 > 抗体 > 未分化胚胎干细胞转录因子1抗体

未分化胚胎干细胞转录因子1抗体

  • 产品货号:mlR12207-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR12207

英文名称 :  UTF1

中文名称 :  未分化胚胎干细胞转录因子1抗体

    :  hUTF 1; hUTF1; Undifferentiated embryonic cell transcription factor 1; UTF 1; UTF1_HUMAN.  

研究领域 :  发育生物学  信号转导  干细胞  转录调节因子  表观遗传学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应  :  Human, Mouse, Rat, Cow,

产品应用 :  WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.

 :  36kDa

细胞定位 :  细胞核

    :  Lyophilized or Liquid

    :  1mg/ml

 :  KLH conjugated synthetic peptide derived from Human UTF1:101-170/341

    :  IgG

纯化方法 :  affinity purified by Protein A

 :  0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件 :  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed :  PubMed

产品介绍 :   UTF1 is a 341 amino acid protein that localizes to the nucleus and is subject to post-translational phosphorylation. Associating with the TFIID complex via an interaction with the TATA box binding protein (TFIID), UTF1 binds to the N-terminal region of ATF-2 and, via this binding, acts as a transcriptional coactivator of ATF-2, thereby enhancing transcriptional activity. Human UTF1 shares 64% homology with its mouse counterpart, suggesting a similar role between species. The gene encoding UTF1 maps to human chromosome 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolmans syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria. 

Function:

Acts as a transcriptional coactivator of ATF2. 

Subunit:

Binds to the N-terminal region of ATF2. Associates with the TFIID complex through interaction with TBP.

Subcellular Location:

Nucleus. 

Post-translational modifications:

Phosphorylated. 

SWISS:

Q5T230

Gene ID:

8433 

Important Note:

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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