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  人才招聘  關于我們  聯系我們
国产精品无码久久综合网,69天堂人成无码麻豆免费视频,国产免费久久精品99久久
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Myosin VIIa/PE-Cy5.5 Conjugated antibody (bs-7761R-PE-Cy5.5)
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-7761R-PE-Cy5.5
英文名稱1 Rabbit Anti-Myosin VIIa/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標記的肌球蛋白7a/常染色體隱性耳聾蛋白2抗體
別    名 Deafness autosomal dominant 11; Deafness autosomal recessive 2; DFNA11; DFNB 2; DFNB2; Myo7a; Myosin 7a; Myosin VIIa; MYU7A; NSRD 2; NSRD2; Ush 1B; Ush1b; Usher syndrome 1B.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 信號轉導  干細胞  細胞骨架  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, )
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 244kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Myosin VIIa
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:
Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. In retina, myosin VIIa may play a role in trafficking of ribbon-synaptic vesicle complexes and renewal of the outer photoreceptors disks. In inner ear, it may maintain the rigidity of stereocilia during the dynamic movements of the bundle.

Function:
Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments. In retina, myosin VIIa might play a role in trafficking of ribbon-synaptic vesicle complexes and renewal of the outer photoreceptors disks. In inner ear, it might maintain the rigidity of stereocilia during the dynamic movements of the bundle. Involved in hair-cell vesicle trafficking of aminoglycosides, which are known to induce ototoxicity.

Subunit:
Interacts with PLEKHB1 (via PH domain). Might homodimerize in a two headed molecule through the formation of a coiled-coil rod. Binds MYRIP and WHRN.

Subcellular Location:
Cytoplasm (Probable). Note=In the photoreceptor cells, mainly localized in the inner and base of outer segments as well as in the synaptic ending region.

Tissue Specificity:
Expressed in the pigment epithelium and the photoreceptor cells of the retina. Also found in kidney, liver, testis, cochlea, lymphocytes. Not expressed in brain.

DISEASE:
Defects in MYO7A are the cause of Usher syndrome type 1B (USH1B) [MIM:276900]. USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa and sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness.
Defects in MYO7A are the cause of deafness autosomal recessive type 2 (DFNB2) [MIM:600060]; also called neurosensory non-syndromic recessive deafness 2 (NSRD2). DFNB2 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Defects in MYO7A are the cause of deafness autosomal dominant type 11 (DFNA11) [MIM:601317].

Similarity:
Contains 2 FERM domains.
Contains 5 IQ domains.
Contains 1 myosin head-like domain.
Contains 2 MyTH4 domains.
Contains 1 SH3 domain.

Database links:
 

UniProtKB/Swiss-Prot: Q13402.2



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: 东北老妇露脸xXXXX| 一级毛片在线直播视频电影| 日日插日日干日日爆 | 边吃奶边拉粑粑是什么情况 | 自慰会得hiv和hpv吗| 无码人妻av免费一区二区三区午夜 | 久久精品国产AV一区二区三区| 成人福利免费视频网站软件 | 中文字幕中文字幕在线观看综合一区二区三区 | 中文字幕人妻无码系列第三区韩| 亚洲国产婷婷综合在线精品中文 | 午夜精品久视频在线观看丝袜美腿91a| 乱人伦人妻中文字幕在线,亚洲性色精品一区二区在线 | 中文字幕亚洲综合久久2,亚洲黄色录像 | 成人啪啪色婷婷久?0?56工厂| 亚洲另类区无码调教| 精品人妻无码在线视频导航| 中文字幕久久精品无码人妻少妇| 人妻少妇偷人精品视频不卡婚外情第二季 | 精品一区二区三区免费毛片爱香蕉视频 | 久久久尹人尹人大香| 中文最新AV第一页| 久久久亚洲中文字幕日韩一区 | 好看中文字幕色视频| 亚洲经典在线中文字幕视频| 国产羞羞视频在线观看的时候 | 国精品无码一区二区三区D七天| 亚洲一区二区三区在线观看ww| 久久精品国产免费观看无遮挡 | 亚洲日韩乱码人人爽人人澡l| 精品久久久久久久久中文字幕_亚洲精品| 永久免费AV无码网站4K国产岛国| 久久99国产乱子伦精品免费,怡红院成永久免费 | 欧美日韩三区四区美女| 中文字幕久久精品无码人妻少妇| 久久精品中文字幕久久天堂| 亚洲综合国产一区二区三区红桃| 国产在线观看无码视频不卡| 无码日韩精品一区二区人妻视频,久久久无码 | 亚洲中文字幕久久无码Va| 国产午夜精品理论片九九九九久久久九九久久久久久 |