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(zhì)量反饋  關于我們  聯(lián)系我們
黄色视频网站大全,国产精品久久久久毛片大屁完整版
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-EDA/Gold Conjugated antibody (bs-12347R-Gold)
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(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-12347R-Gold
英文名稱 Rabbit Anti-EDA/Gold Conjugated antibody
中文名稱 膠體金標記的外胚層發(fā)育不良蛋白1抗體
別    名 Ectodysplasin A, membrane form; Ectodermal dysplasia 1, anhidrotic; Ectodermal dysplasia protein; Ectodermal dysplasia, anhidrotic (hypohydrotic); Ectodysplasin A; ECTODYSPLASIN A1 ISOFORM; ECTODYSPLASIN A2 ISOFORM; ECTODYSPLASIN; Ectodysplasin-A; ED1 A1; ED1 A2; ED1; ED1 GENE; Eda A1; Eda A2; eda; EDA protein; EDA protein homolog; EDA_HUMAN; EDA1; EDA1 GENE; EDA2; HED; ODT1; Oligodontia 1; STHAGX1; Ta; Tabby; Tabby protein; X linked anhidroitic ectodermal dysplasia protein; XHED; XLHED.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 細胞生物  發(fā)育生物學  信號轉(zhuǎn)導  干細胞  細胞膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse,  (predicted: Human, Rat, Cow, )
產(chǎn)品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 41kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Ectodysplasin-A, membrane form
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
Affected males of X-linked anhidrotic ectodermal dysplasia show hypotrichosis, abnormal teeth and absent sweat glands. Some of the patients reported by Halperin and Curtis showed mental defect also, but this is not an invariable feature. Ectodysplasin A (EDA) is a trimeric type II membrane protein that co-localizes with cytoskeletal structures at the lateral and apical surfaces of cells. EDA is expressed in hair follicles and in the epidermis of adult skin. The sequence of the longest isoform includes an interrupted collagenous domain of 19 Gly-X-Y repeats and a motif conserved in the tumor necrosis factor (TNF)-related ligand family. EDA is a member of the TNF-related ligand family involved in the early epithelial-mesenchymal interaction that regulates ectodermal appendage formation. Similar to other members of collagenous membrane proteins and members of TNF-related ligands, EDA is a type II membrane protein which forms trimers.

Function:
Seems to be involved in epithelial-mesenchymal signaling during morphogenesis of ectodermal organs. Isoform 1 binds only to the receptor EDAR, while isoform 3 binds exclusively to the receptor XEDAR.

Subunit:
Homotrimer. The homotrimers may then dimerize and form higher-order oligomers.

Subcellular Location:
Secreted and Cell membrane.

Tissue Specificity:
Not abundant; expressed in specific cell types of ectodermal (but not mesodermal) origin of keratinocytes, hair follicles, sweat glands. Also in adult heart, liver, muscle, pancreas, prostate, fetal liver, uterus, small intestine and umbilical chord.

Post-translational modifications:
N-glycosylated.
Processing by furin produces a secreted form.

DISEASE:
Defects in EDA are the cause of ectodermal dysplasia type 1 (ED1) [MIM:305100]; also known as Christ-Siemens-Touraine syndrome or X-linked hypohidrotic ectodermal dysplasia (XLHED). Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ED1 is a disease characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. ED1 is the most common form of over 150 clinically distinct ectodermal dysplasias.
Defects in EDA are the cause of tooth agenesis selective X-linked type 1 (STHAGX1) [MIM:313500]. A form of selective tooth agenesis, a common anomaly characterized by the congenital absence of one or more teeth. Selective tooth agenesis without associated systemic disorders has sometimes been divided into 2 types: oligodontia, defined as agenesis of 6 or more permanent teeth, and hypodontia, defined as agenesis of less than 6 teeth. The number in both cases does not include absence of third molars (wisdom teeth).

Similarity:
Belongs to the tumor necrosis factor family.
Contains 1 collagen-like domain.

Database links:

Entrez Gene: 1896 Human

Entrez Gene: 13607 Mouse

Omim: 300451 Human

SwissProt: Q9BEG5 Cow

SwissProt: Q92838 Human

SwissProt: O54693 Mouse

Unigene: 105407 Human

Unigene: 328086 Mouse



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.nmgps.com 北京博奧森生物技術有限公司
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
538prom精品视频任你爽 | 四lll少妇BBBB槡BBBB | 蜜桃视频一区二区三区四区软件介绍 | 亚洲性猛交XXXX乱大交 | 日本无码一区二区蜜桃小说 | 同学吃我的奶我流水了 | 农村嫩苞一区二区三区视频 | 西西4444WWW无码视频 | 亚洲视频免费在线观看 | 天天干天天日夜夜吻 | 国产精品一区二区久久精品爱微奶 | 久久久久国产精品无码免费看 | 日本免费AAAAAAAA直播片 | 国产色情无码A片爆乳直播 91人妻无码成人精品一区 | 亚洲黄色视频免费在线观看 | 久久天天躁狠狠躁夜夜av | 中文字字幕在线中文 | 日本无码中文字幕乱偷在线 | 四虎永久免费在线观看 | 亚洲AV色香蕉一区二区三区老师 | 国产福利在线观看 | 午夜在线免费视频 | 国产在线拍揄自揄拍无码视频 | 国产精品久久久久久蜜臀男女双修 | 一级人体A片免费观看 | 日本五十路熟妇视频 | 国产一级片免费观看 | 国产精品福利一区二区三区四季 | 一区二区三区无码高清 | 久久久久亚洲AV无码尤物黑人 | 少妇被黑人到高潮喷白浆 | 国产成人精品一区二区色戒 | 欧美偷伦无码一区二区 | 红桃视频一区二区三区 | 夜夜躁狠狠躁日日躁av | 亚洲视频一区二区 | 欧美日韩高清免费观看 | 亚洲精品乱码久久久久久蜜桃麻豆 | 潮喷 合集 喷水 mp4 | 农村妇女躁BBBB高朝喷水电影 | 国产一区二区视频在线 |