亚洲制服欧美另类-午夜激情av电影-日本高清中文字幕一区二区三区-中国欧美日韩一区二区三区-欧洲亚洲日本韩国-成人欧美激情一区二区-亚洲偷偷自拍高清

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
国产精品久久久久久精品毛片,乱码精品一区二区三区,成人女人a毛片在线看
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Desmocollin 2 + 3/BF350 Conjugated antibody (bs-2983R-BF350)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-2983R-BF350
英文名稱 Rabbit Anti-Desmocollin 2 + 3/BF350 Conjugated antibody
中文名稱 BF350標記的橋粒糖蛋白2/橋粒糖蛋白3抗體
別    名 ARVD11; Cadherin family member 2; CDHF2; Desmocollin 3; Desmocollin3; Desmocollin-2; Desmocollin-3; Desmocollin2; Desmosomal glycoprotein II and III; Desmosomal glycoprotein II; Desmosomal glycoprotein II/III; Desmosomal glycoprotein III; DG2; DGII/III; DKFZp686I11137; DSC 2; DSC2; DSC2_HUMAN; DSC3.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 心血管  細胞生物  信號轉(zhuǎn)導  細胞粘附分子  細胞表面分子  細胞骨架  細胞外基質(zhì)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Horse, )
產(chǎn)品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 84kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Desmocollin 2
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(chǎn)品介紹 background:
The protein encoded by this gene is a calcium-dependent glycoprotein that is a member of the desmocollin subfamily of the cadherin superfamily. These desmosomal family members, along with the desmogleins, are found primarily in epithelial cells where they constitute the adhesive proteins of the desmosome cell-cell junction and are required for cell adhesion and desmosome formation. The desmosomal family members are arranged in two clusters on chromosome 18, occupying less than 650 kb combined. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia-11. Alternative splicing results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

Function:
Component of intercellular desmosome junctions. Involved in the interaction of plaque proteins and intermediate filaments mediating cell-cell adhesion. May contribute to epidermal cell positioning (stratification) by mediating differential adhesiveness between cells that express different isoforms.

Subunit:
Interacts with DSP, PKP2 and JUP.

Subcellular Location:
Cell membrane; Single-pass type I membrane protein. Cell junction, desmosome.

Tissue Specificity:
In all epithelia tested and heart.

DISEASE:
Defects in DSC2 are the cause of familial arrhythmogenic right ventricular dysplasia type 11 (ARVD11) [MIM:610476]; also known as arrhythmogenic right ventricular cardiomyopathy 11 (ARVC11). ARVD is an autosomal dominant disease characterized by partial degeneration of the myocardium of the right ventricle, electrical instability, and sudden death. It is clinically defined by electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elements, preferentially involve the right ventricular free wall.

Similarity:
Contains 5 cadherin domains.

Database links:

Entrez Gene: 1824 Human

Entrez Gene: 1825 Human

Omim: 125645 Human

Omim: 600271 Human

SwissProt: Q02487 Human

SwissProt: Q14574 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Involvement in disease:Defects in DSC2 are the cause of familial arrhythmogenic right ventricular dysplasia type 11 (ARVD11); also known as arrhythmogenic right ventricular cardiomyopathy 11 (ARVC11). ARVD is an autosomal dominant disease characterized by partial degeneration of the myocardium of the right ventricle, electrical instability, and sudden death. It is clinically defined by electrocardiographic and angiographic criteria; pathologic findings, replacement of ventricular myocardium with fatty and fibrous elements, preferentially involve the right ventricular free wall.
版權(quán)所有 2004-2026 www.a6308.cn 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)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(wǎng)安備110107000727號
免费国产成人高清在线网站东京 | a级毛片免费全部播放无码 日韩久久久久精品一区二区三区 | 色一情一乱一伦一区二区三区 | 久久国产精品偷任你爽任你A | 动漫人物自慰喷水网站 | 国产后入又长又硬 | 真人短片20分钟以上 | 好涩啊揉爆骚奶的视频 | 99久在线国内在线播放免费观看 | 国产91成人精品流白浆 | 欧美亚洲精品中文字幕乱码免费高清 | 一级毛片免费在线播放 | 久久永久免费视频 | 插B内射18免费视频 内射无套在线观看高清完整免费 | 国产大屁股喷水视频在线 | 日韩欧美一中文字慕2O22 | 2018国产精华国产精品 | 国产精品免费大片 | 性高湖久久久久久久久 | 欧美一区二区高清 | XXX2高清在线观看免费视频 | 一木道一二三区精品 | 国产片AV片永久免费观看 | 久久久高清国产999尤物 | 特黄四级人牲片在线观看 | 中文美女乱婬试看视频 | 国产一区内射最近更新 | 精品日韩乱码久久久久久 | 亚洲精品无码a√中文字幕网站 | 亚洲国产精品人人爽夜夜爽 | 日本视频在线免费 | 久久久成人免费高清一区二区三区视频不卡 | 好涩啊揉爆骚奶的视频 | 欧美人与拘牲交大全O人禾 天天躁日日躁狠狠躁日日躁黑人 | 女人被狂躁到高潮视频免费 | 18禁止看的免费污网站 | 亚洲日韩国产精品乱-久 | 无码专区—VA亚洲V天堂 | 天美传媒TMY0013在线观看 | 一级毛片久久久久久久女人18 | 夜夜添无码试看一区二区三区 |