<small id="pxpuz"><tbody id="pxpuz"><noframes id="pxpuz"></noframes></tbody></small>

  1. <noscript id="pxpuz"><tbody id="pxpuz"></tbody></noscript>
        • <td id="pxpuz"><tr id="pxpuz"><th id="pxpuz"></th></tr></td>
        • <small id="pxpuz"><tbody id="pxpuz"><noframes id="pxpuz"></noframes></tbody></small>

            <noscript id="pxpuz"><dl id="pxpuz"></dl></noscript>
              <source id="pxpuz"><tr id="pxpuz"></tr></source>

              精品乱子伦一区二区三区_亚洲精品乱码久久久久久按摩_亚洲久久久久久久_日韩av亚洲欧美一区二区三区_来一水AV@lysav

              免費(fèi)咨詢熱線

              15121004110

              資料下載

              DATA DOWNLOAD

              當(dāng)前位置:首頁(yè)資料下載UTF1抗原,未分化胚胎干細(xì)胞轉(zhuǎn)錄因子1抗原

              UTF1抗原,未分化胚胎干細(xì)胞轉(zhuǎn)錄因子1抗原

              發(fā)布時(shí)間:2024/12/18點(diǎn)擊次數(shù):27

              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.

               

               


              文件下載    

              掃碼加微信

              服務(wù)熱線

              021-34553900

              上海市青浦區(qū)

              562398366@qq.com

              Copyright © 2024上海允麥生物科技有限公司 All Rights Reserved    備案號(hào):滬ICP備20013035號(hào)-2

              技術(shù)支持:化工儀器網(wǎng)    管理登錄    sitemap.xml

              精品乱子伦一区二区三区_亚洲精品乱码久久久久久按摩_亚洲久久久久久久_日韩av亚洲欧美一区二区三区_来一水AV@lysav
              <small id="pxpuz"><tbody id="pxpuz"><noframes id="pxpuz"></noframes></tbody></small>

              1. <noscript id="pxpuz"><tbody id="pxpuz"></tbody></noscript>
                    • <td id="pxpuz"><tr id="pxpuz"><th id="pxpuz"></th></tr></td>
                    • <small id="pxpuz"><tbody id="pxpuz"><noframes id="pxpuz"></noframes></tbody></small>

                        <noscript id="pxpuz"><dl id="pxpuz"></dl></noscript>
                          <source id="pxpuz"><tr id="pxpuz"></tr></source>
                          涪陵区| 巴彦淖尔市| 乐都县| 新竹县| 富顺县| 海南省| 乐陵市| 大方县| 仙桃市| 潍坊市| 延边| 新建县| 西华县| 霍山县| 林州市| 孟村| 昌图县| 玛曲县| 松阳县| 嘉黎县| 于都县| 内乡县| 洛宁县| 宝兴县| 和林格尔县| 霍林郭勒市| 西峡县| 浦城县| 舒城县| 洛南县| 榆社县| 左贡县| 安阳县| 陆丰市| 河源市| 白水县| 泰安市| 望城县| 清水县| 都江堰市| 淳安县|