四虎国产精品成人免费影视_国产亚洲精品美女久久久久久久久久_亚洲国产精品日韩_成人精品在线

今天是2025年6月21日 星期六,歡迎光臨本站 上海研生實業有限公司 網址: www.youjlzzxxx.com

一抗

8號染色體開放閱讀框31抗體

文字:[大][中][小] 2017-5-4    瀏覽次數:1381    


英文名稱  Anti-C8orf31 
中文名稱  8號染色體開放閱讀框31抗體 
別    名  Chromosome 8 open reading frame 31; Uncharacterized protein C8orf31; CH031_HUMAN.  

詳細介紹:


濃    度  1mg/1ml 
規 格  0.2ml/200μg  
抗體來源  Rabbit  
克隆類型  polyclonal 
交叉反應  Human   
產品類型  一抗    
研究領域  細胞生物 免疫學  
蛋白分子量  predicted molecular weight: 15kDa 
性    狀  Lyophilized or Liquid 
免 疫 原  KLH conjugated synthetic peptide derived from human C8orf31 
亞    型  IgG 
純化方法  affinity purified by Protein A 
儲 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4 
產品應用   WB=1:100-500  ELISA=1:500-1000  IP=1:20-100  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500 
(石蠟切片需做抗原修復) 
 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user.  
保存條件  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. 
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

相關資料:


產品介紹 Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf31 gene product has been provisionally designated C8orf31 pending further characterization.
Database links : UniProtKB/Swiss-Prot: Q8N9H6.1



返回上一步
打印此頁
[向上]

網站首頁

公司介紹

產品中心

技術服務

技術文獻

在線留言

聯系我們

在線客服

售前咨詢

售后服務

咨詢電話:
021-59989018

請掃描二維碼
打開手機站

主站蜘蛛池模板: 荔波县| 临澧县| 沙雅县| 田林县| 建德市| 嵊州市| 通许县| 寿阳县| 达日县| 依兰县| 大姚县| 饶阳县| 资兴市| 陇西县| 盐边县| 碌曲县| 镇原县| 岳阳市| 子长县| 阿勒泰市| 新巴尔虎左旗| 仲巴县| 神池县| 永定县| 枞阳县| 惠东县| 徐闻县| 德保县| 神池县| 武定县| 周宁县| 留坝县| 遂川县| 依兰县| 黔江区| 奉贤区| 云南省| 富锦市| 阳西县| 紫阳县| 黄骅市|