mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關(guān)注公眾號(hào)           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
欧美成人tv在线播放,日韩欧美中文字幕人妻
Rabbit Anti-gamma catenin/BF594 Conjugated antibody (bs-1720R-BF594)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.p2b3.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.p2b3.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-1720R-BF594
英文名稱 Rabbit Anti-gamma catenin/BF594 Conjugated antibody
中文名稱 BF594標(biāo)記的γ連環(huán)蛋白/Catenin γ /γ鏈接素抗體
別    名 ARVD 12; ARVD12; Catenin (cadherin associated protein) gamma 80kDa; Catenin (cadherin associated protein), gamma 80kDa; catenin (cadherin-associated protein) gamma (80kD); Catenin gamma 80kDa; Catenin gamma; CTNNG; Desmoplakin 3; Desmoplakin III; Desmoplakin-3; Desmoplakin3; DesmoplakinIII; DP 3; DP III; DP3; DPIII; Gamma catenin; Junction plakoglobin; JUP; OTTHUMP00000164732; OTTHUMP00000164735; OTTHUMP00000164738; PDGB; PKGB; PLAK_HUMAN; PLAKOGLOBIN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞骨架  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
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 82kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Cateninma gamma
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.
產(chǎn)品介紹 background:
This gene encodes a major cytoplasmic protein which is the only known constituent common to submembranous plaques of both desmosomes and intermediate junctions. This protein forms distinct complexes with cadherins and desmosomal cadherins and is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat. Mutation in this gene has been associated with Naxos disease. Alternative splicing occurs in this gene; however, not all transcripts have been fully described. [provided by RefSeq].

Function:
Common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of plakoglobin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques. Acts as a substrate for VE-PTP and is required by it to stimulate VE-cadherin function in endothelial cells. Can replace beta-catenin in E-cadherin/catenin adhesion complexes which are proposed to couple cadherins to the actin cytoskeleton.

Subunit:
Cell junction, adherens junction. Cell junction, desmosome. Cytoplasm, cytoskeleton. Membrane; Peripheral membrane protein. Note=Cytoplasmic in a soluble and membrane-associated form.

Subcellular Location:
Cell junction, adherens junction. Cell junction, desmosome. Cytoplasm, cytoskeleton. Membrane. Cytoplasmic in a soluble and membrane-associated form.

Post-translational modifications:
May be phosphorylated by FER.

DISEASE:
Defects in JUP are the cause of Naxos disease (NXD) [MIM:601214]. NXD is an autosomal recessive disorder combining diffuse non-epidermolytic palmoplantar keratoderma with arrhythmogenic right ventricular dysplasia/cardiomyopathy and woolly hair.
Defects in JUP are the cause of familial arrhythmogenic right ventricular dysplasia type 12 (ARVD12) [MIM:611528]; also called arrhythmogenic right ventricular cardiomyopathy 12 (ARVC12). 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:
Belongs to the beta-catenin family.
Contains 9 ARM repeats.

Database links:

Entrez Gene: 3728 Human

Entrez Gene: 16480 Mouse

Entrez Gene: 81679 Rat

Omim: 173325 Human

SwissProt: P14923 Human

SwissProt: Q02257 Mouse

SwissProt: Q6P0K8 Rat

Unigene: 514174 Human

Unigene: 299774 Mouse

Unigene: 11255 Rat



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

細(xì)胞骨架的微絲E-cad通過(guò)相關(guān)蛋白α、β、γ-cat經(jīng)羥基端在細(xì)胞內(nèi)與細(xì)胞骨架的微絲連接形成E-cad/cat)復(fù)合體,參與細(xì)胞粘附、生長(zhǎng)、增殖等過(guò)程.
版權(quán)所有 2004-2026 www.www.p2b3.cn 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
亚洲日韩不卡一区二区三区| 日本高清一区二区三区在线观看| 亚洲乱熟女一区二区三区| 麻豆视频一级片在线观看| 好嗨哟直播看片在线观看| 九九视频这里只有精品| 一级做a爱过程免费视频俩| 国产日女人视频在线观看| 欧美日韩在线成人| 美女爽的嗷嗷叫免费| 国产精品毛片无遮挡高清| 色综合色狠狠天天综合色| 骚女性爱视频在线看| 西瓜在线看免费观看视频| 日本男人捅女人机机| 午夜精品福利一区二区三区蜜桃p| 一区二中文字幕在线看国产一区| 美女被插b在线观看| 91成人精品国语自产拍| 美女主播被操流水| 国产乱精品一区二区三区视频了| 老司机免费福利午夜入口| 老湿机69福免费破解版| 欧美区 日韩区 亚洲区| 久久久中文字幕在线视频| 欧美人与动人物A级| 久久久久人妻一区精品加勒比| 黑大吊肏小騷逼噴水| 日韩毛片一区视频免费在线观看| 亚洲国产成人手机版| 男生鸡鸡插进女生笑穴里| 搞段B片黄色全免费看看| 国产精品一区二区三区在线视| 毛片日产av一区二区三区四区| 色橹橹欧美在线观看视频高清免费| 国产熟女视频一区二区三区| 日本成人在线一区中文字幕| 亚洲精品国产人久久| 亚洲AV天堂一区二区香蕉| 日韩欧美一二三区| 美女被插进去黄色|