亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯系我們
久久精品亚洲欧美va,色婷婷综合激情视频免费看,男人扒开女人下面狂躁动漫版
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-C11ORF16/RBITC Conjugated antibody (bs-9935R-RBITC)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-9935R-RBITC
英文名稱 Rabbit Anti-C11ORF16/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的11號染色體開放閱讀框16抗體
別    名 Chromosome 11 open reading frame 16; Hypothetical protein LOC56673; Uncharacterized protein C11orf16; CK016_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  細胞周期蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 52kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C11ORF16
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
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.
產品介紹 background:
C11orf16 is a 404 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 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-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. 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.

Database links:

Entrez Gene: 56673 Human

SwissProt: Q9NQ32 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 国产亚洲精品无码成人一| 国产三级精品久久国产三级| 久久国产真实乱对白按摩内容| 亚洲综合国产一区二区三区红桃| Av中文字幕网站高溯| 被夫上司糟蹋在线观看免费视频 | 国产成人精品AA毛片虐男| 黑人巨大20P| 国产免费一区二区三区免费视频苏语棠| 久久精品国产亚洲精品红樱app| 久久久久99精品成人片,美女遮不挡... | 伦理片中文字幕完整视频| 日日久视频日日久| 蜜臀av性久久久久蜜臀aⅴ涩爱| 精品国产日韩热久久简单Av| 国产一级做a爰片在线看免费hong t ao t v | 精品国产一区二区25P| 中文字幕无码久久久精密桃| 伊人中出人妻| 无码中文人妻视频2019| 熟女人妻久久久一区二区蜜桃老牛| 天堂成人小说视频首页| 国产日本Av电影合集| 亚洲青青久久人综合| 天堂国产一区二区三区资源| 国产美女久久精品香蕉精品 | 亚洲一卡一卡二新区无人区的观看体验| 亚洲制服丝袜第一页波多野| 久久久国产乱子伦精品 最新章节| 18禁网站免费无遮挡无码中文_日韩欧美中文| 中文字幕亚洲综合久久99| 男女无遮挡吃奶视频| 国产丝袜调教视频足j| 亚洲国产专区一区二区麻豆99视频| 无码人妻少妇色欲AV一区二区| 国产成人无码18禁午夜福利p时刻 国产成人无码18禁午夜福利网址木青 | 亚洲成a人片在线观看无码sm粗口 亚洲成a人片在线观看无码粗暴 | 无码中文字幕日韩专区,亚| 国产电影午夜成年免费视频| 伸手进去?的我好爽无码| 久久大香伊蕉在人线国产H_女人高潮抽|