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UTF1抗原,未分化胚胎干細(xì)胞轉(zhuǎn)錄因子1抗原

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  • 瀏覽次數(shù)

    17次
  • 上傳時(shí)間

    2024年12月18日
關(guān)鍵詞
UTF1,UTF1抗體,未分化胚胎干細(xì)胞轉(zhuǎn)錄因子1,未分化胚胎干細(xì)胞轉(zhuǎn)錄因子1抗體,重組蛋白
上傳者
上海允麥生物科技有限公司
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資料簡(jiǎn)介

Recombinant human UTF1   

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

濃度:1mg/ ml

來(lái)源:Recombinant Human

純度:≥95% SDS-PAGE

表達(dá)系統(tǒng):Escherichia coli

標(biāo)簽:His tag  

蛋白長(zhǎng)度:Full length protein

內(nèi)毒素水平:<1.000 Eu/µg

純化方法:HPLC

應(yīng)用:SDS-PAGE,Western blot,ELISA

Biological activity,immunology research

保存:-20℃

保質(zhì)期:1年

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, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

 


抗體

產(chǎn)品名稱:Rabbit Anti-UTF1 antibody

Rabbit Anti-UTF1  

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

來(lái)源:Rabbit

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反應(yīng):Human (predicted: Mouse,Rat,Cow)

理論分子量:36kDa

免疫原:KLH conjugated synthetic peptide derived from Human UTF1 

保存:-20
保質(zhì)期:1

 

單克隆抗體

產(chǎn)品名稱:Anti-UTF1 antibody

Mouse Anti-UTF1 

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

來(lái)源:Mouse

克隆類型:Monoclonal

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反應(yīng): Human 

理論分子量:36kDa

免疫原:KLH conjugated synthetic peptide derived from Human UTF1  

保存:-20
保質(zhì)期:1

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, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

 

 


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