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UTF1抗體,未分化胚胎干細胞轉錄因子1抗體

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  • 上傳時間

    2024年12月18日
關鍵詞
UTF1,UTF1抗原,重組蛋白 ,未分化胚胎干細胞轉錄因子1,未分化胚胎干細胞轉錄因子1抗原
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資料簡介

產品名稱:Rabbit Anti-UTF1 antibody

Rabbit Anti-UTF1  

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

來源:Rabbit

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

應用: 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: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
保質期:1

 

單克隆抗體

產品名稱:Anti-UTF1 antibody

Mouse Anti-UTF1 

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

來源:Mouse

克隆類型:Monoclonal

濃度:1mg/ml

亞型:IgG

應用: 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: Human 

理論分子量:36kDa

免疫原:KLH conjugated synthetic peptide derived from Human UTF1  

保存:-20
保質期: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.

 

 

Recombinant human UTF1   

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

濃度:1mg/ ml

來源:Recombinant Human

純度:≥95% SDS-PAGE

表達系統:Escherichia coli

標簽:His tag  

蛋白長度:Full length protein

內毒素水平:<1.000 Eu/µg

純化方法:HPLC

應用:SDS-PAGE,Western blot,ELISA

Biological activity,immunology research

保存:-20℃

保質期: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.


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