欧美日韩三区四区_试看120秒一区二区三区_亚洲一区二区在线观看视频_久久综合色88

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.845158.com

標記一抗

FITC標記的錨蛋白重復結構域蛋白13B抗體

文字:[大][中][小] 2017-5-2    瀏覽次數:994    

                              FITC標記的錨蛋白重復結構域蛋白13B抗體                                                                                                                                                
英文名稱Anti-ANKRD13B/FITC
中文名稱:FITC標記的錨蛋白重復結構域蛋白13B抗體
別    名Ankrd13b; ANKRD13B(ankyrin repeat domain 13B); ankyrin repeat domain 13B; AN13B_HUMAN.  

詳細介紹:


規格:100ul 
說 明 書100ul  
研究領域細胞生物  免疫學  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應 Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit, 
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70kDa
性    狀Lyophilized or Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human ANKRD13B
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.

相關資料:


產品介紹background:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes can lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD13B (ankyrin repeat domain 13B) is a 626 amino acid protein that contains two ANK repeats and three ubiquitin-interacting motif (UIM) repeats. Conserved in dog, cow, mouse and rat, ANKRD13B exists as two alternatively spliced isoforms. The gene that encodes ANKRD13B maps to human chromosome 17, which makes up over 2.5% of the human genome, with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. BRCA1 is recognized as a genetic determinant of early onset breast cancer. Chromosome 17 is also linked to neurofibromatosis, dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.

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: 道真| 同江市| 中江县| 利川市| 衢州市| 西宁市| 城口县| 霍城县| 凯里市| 四子王旗| 和硕县| 库尔勒市| 永吉县| 布尔津县| 龙里县| 普陀区| 金塔县| 虞城县| 凌源市| 齐齐哈尔市| 延津县| 唐海县| 获嘉县| 宣威市| 波密县| 海门市| 新建县| 翁牛特旗| 洱源县| 库车县| 五原县| 齐齐哈尔市| 铅山县| 岳西县| 桃源县| 慈溪市| 环江| 南丹县| 龙泉市| 禄劝| 邳州市|