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當(dāng)前位置:華瑞科研網(wǎng)-ELISA試劑盒>>科研抗體>>科研一抗>>Anti-BATF2抗體,BATF2蛋白抗體科研

Anti-BATF2抗體,BATF2蛋白抗體科研

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所  在  地上海市

聯(lián)系方式:韓經(jīng)理查看聯(lián)系方式

更新時間:2018-05-04 23:30:25瀏覽次數(shù):304次

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商鋪產(chǎn)品:9992條

所在地區(qū):上海上海市

聯(lián)系人:韓經(jīng)理 (銷售)

產(chǎn)品簡介

“Anti-BATF2抗體,BATF2蛋白抗體科研"我公司擁有*的細(xì)胞服務(wù)技術(shù),*的儀器設(shè)備和專業(yè)的ELISA檢測試劑盒、生物索標(biāo)記、熒光索標(biāo)記、酶標(biāo)記等,廣泛用于多種分析研究與技術(shù)測定。咨詢,我們將竭誠為你服務(wù)!

詳細(xì)介紹

Anti-BATF2抗體,BATF2蛋白抗體科研產(chǎn)品介紹:

BATF2 is a 274 amino acid protein that localizes to the nucleus and contains one bZIP domain, suggesting that it may be involved in transcriptional regulation. The gene encoding BATF2, which is expressed as multiple alternatively spliced isoforms, is located on human chromosome 11. With approximay 135 million base pairs and 1,400 genes, chromosome 11 comprises approximay 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-angiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes. 


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產(chǎn)品詳情:
產(chǎn)品編號:HRK-18913R
產(chǎn)品規(guī)格: 0.1ml/0.2ml
產(chǎn)品別名:B ATF 2; Basic leucine zipper transcriptional factor ATF like 2; BATF2; BATF2_HUMAN; MGC20410; SARI; Suppressor of AP 1 regulated by IFN
產(chǎn)品價格:詢價(電詢或客服)
產(chǎn)品用途:科研實驗
貯 存:   貯存于-20℃.

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