强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關于我們  聯(lián)系我們
四lll少妇BBw搡BBBB槡BBBB ,国产成人a亚洲精品,天美传媒妇乱XXXXX
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Desmocollin 2 + 3/BF647 Conjugated antibody (bs-2983R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-2983R-BF647
英文名稱 Rabbit Anti-Desmocollin 2 + 3/BF647 Conjugated antibody
中文名稱 BF647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  
研究領域 心血管  細胞生物  信號轉導  細胞粘附分子  細胞表面分子  細胞骨架  細胞外基質  
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.
版權所有 2004-2026 nmgps.com 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(yī)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(wǎng)安備110107000727號
亚洲熟伦熟女新五十路熟妇 | 国产成人精品 视频 | 午夜剧场 成人 av | 色欲狠狠躁天天躁无码中文字幕 | 波多野吉衣成人在线 | 在线观看丰满美女100%露胸网站 | 国产A级毛片久久久久 | 欧美mv日韩mv国产网站 | 国产一区二区在线免费观看 | 北条麻妃A片在线播放 | 波多野结衣无码欧洲 | 真人做爰A片免费观看茄子视频 | 特级做a爰片毛片大巴一 | 国产农村成人精品一区 | 国产一级毛片一级A片酒瓶 五十老熟妇乱子伦免费章节 | 在线国产一区二区 | 激情五月天综合网 | 91午夜理伦私人影院 | 欧美性受XXXX黑人XYX性爽 | 一级特黄女人18毛片免费视频 | 水蜜桃秘 蜜桃在线观看 | 91极品美女裸身网站直播 | 特级西西人体444w w w | 国产又黄又爽又色的免费蜜乳 | 久久丫精品忘忧草西安产品 | 日本五十路熟妇视频 | 日本丰满脂肪人人爱视频在线观看50路 | 性XXXX18精品A片 | 人爽人澡人妻A片精品二区 国产农村妇女一区二区三区 | 疯狂欧美大伦交的历史 | 不卡的在线免费视频 | 男人天堂高清无码 | 搡老女人老妇女老熟女60 | 搡老女人老妇老熟女 | 在线免费观看一级毛片 | 新sss在线观看丝 | 西西一级AAA片婬片免费 | 欧美精品1区2区3区 国内揄拍国内精品久久 | 亚洲高清无码中文视频 | 日本一区二三区水蜜桃下载 | 四川一级毛毛片免费网站 |