国产av一区二区三区日韩-人人色在线视频播放-欧美xxxx做受欧美-女人被弄到高潮的免费视频-国产人妻精品一区二区三区-男女猛烈xx00免费视频试看

今天是2024年12月28日 星期六,歡迎光臨本站 上海研生實業(yè)有限公司 網(wǎng)址: shuajiwang.cn

標記一抗

FITC標記的錨蛋白重復結構域蛋白22抗體

文字:[大][中][小] 2017-5-2    瀏覽次數(shù):1115    

                              FITC標記的錨蛋白重復結構域蛋白22抗體                                                                                                                                                
英文名稱Anti-ANKRD22/FITC
中文名稱:FITC標記的錨蛋白重復結構域蛋白22抗體
別    名Ankrd22; Ankyrin repeat domain 22; Ankyrin repeat domain-containing protein 22; ANR22_HUMAN.  

詳細介紹:


規(guī)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, Dog, Pig, Cow, Horse, Rabbit, Sheep, 
產(chǎn)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22kDa
性    狀Lyophilized or Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human ANKRD22
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(chǎn)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 lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in 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.

返回上一步
打印此頁
[向上]

網(wǎng)站首頁

公司介紹

產(chǎn)品中心

技術服務

技術文獻

在線留言

聯(lián)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