日本久久精品,韩国成人免费视频,51国产成人精品午夜福中文下载,成人毛片老司机大片

今天是2025年5月10日 星期六,歡迎光臨本站 上海研生實(shí)業(yè)有限公司 網(wǎng)址: www.a3kkk.com

標(biāo)記一抗

FITC標(biāo)記的錨蛋白重復(fù)結(jié)構(gòu)域蛋白20A3抗體

文字:[大][中][小] 2017-5-2    瀏覽次數(shù):1221    

                              FITC標(biāo)記的錨蛋白重復(fù)結(jié)構(gòu)域蛋白20A3抗體                                                                                                                                                
英文名稱Anti-ANKRD20A3/FITC
中文名稱:FITC標(biāo)記的錨蛋白重復(fù)結(jié)構(gòu)域蛋白20A3抗體
別    名Ankyrin repeat domain 20 family member A3; Ankyrin repeat domain 20A related; Ankyrin repeat domain containing protein 20A3; MGC176486; MGC198508; A20A3_HUMAN.  

詳細(xì)介紹:


規(guī)格:100ul 
說(shuō) 明 書100ul  
研究領(lǐng)域細(xì)胞生物  免疫學(xué)  
抗體來(lái)源Rabbit
克隆類型Polyclonal
交叉反應(yīng) Human, 
產(chǎn)品應(yīng)用IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量94kDa
性    狀Lyophilized or Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human ANKRD20A3
亞    型IgG
純化方法affinity purified by Protein A
儲(chǔ) 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(guān)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. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias

返回上一步
打印此頁(yè)
[向上]

網(wǎng)站首頁(yè)

公司介紹

產(chǎn)品中心

技術(shù)服務(wù)

技術(shù)文獻(xiàn)

在線留言

聯(lián)系我們

在線客服

售前咨詢

售后服務(wù)

咨詢電話:
021-59989018

請(qǐng)掃描二維碼
打開手機(jī)站

主站蜘蛛池模板: 平度市| 荥阳市| 焦作市| 邳州市| 稷山县| 潞西市| 东阳市| 平原县| 长沙县| 神池县| 双流县| 云霄县| 精河县| 辽中县| 连云港市| 观塘区| 明水县| 静安区| 阳原县| 赣州市| 邹平县| 会昌县| 荣成市| 浮山县| 苍梧县| 周至县| 汶上县| 和田市| 梅州市| 松阳县| 寿宁县| 澎湖县| 长乐市| 驻马店市| 华池县| 施甸县| 布拖县| 西充县| 临朐县| 东明县| 托克逊县|