91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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
久久99精品国产.久久久久久,三人成全免费观看电视剧高清完整版,中文字幕无码在线
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-EDAR/Cy3 Conjugated antibody (bs-13050R-Cy3)
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-13050R-Cy3
英文名稱 Rabbit Anti-EDAR/Cy3 Conjugated antibody
中文名稱 Cy3標記的腫瘤壞死因子受體超家族成員EDAR抗體
別    名 Anhidrotic ectodysplasin receptor 1; DL; Downless (mouse) homolog; Downless homolog; Downless mouse homolog of; Ectodermal dysplasia receptor; Ectodysplasin 1 anhidrotic receptor; Ectodysplasin A receptor; Ectodysplasin-A receptor; ED 1R; ED 3; ED 5; ED1R; ED3; ED5; EDA 1R; EDA 3; EDA A1 receptor; EDA A1R; EDA-A1 receptor; EDA1R; EDA3; Edar; EDAR_HUMAN; HRM1; Tumor necrosis factor receptor superfamily member EDAR.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  生長因子和激素  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Rabbit, )
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 46kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human EDAR
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 tumor necrosis factor receptor (TNFR) superfamily represents a growing family of type I transmembrane glycoproteins that are involved in various cellular functions, including proliferation, differentiation and programmed cell death. These proteins share homology for cysteine-rich repeats in the extracellular ligand binding domain and an intracellular death domain. Members of the TNFR superfamily transmit signals through protein-protein interactions, and these signals can lead to the activation of either the caspase and Jun kinase pathways, which promote cell death, or the NFκB pathway, which results in cell survival. The ectodermal dysplasia receptor (EDAR) promotes all three of these pathways and mediates ectodermal differentiation. EDAR is encoded by the downless gene and is mutated in ectodermal dysplasia syndromes, which are characterized by impaired hair, teeth and sweat gland development. Ectodysplasin A (EDA) is a type II membrane protein that is encoded by the Tabby gene and produces many splice variants, the longest of which, EDA-A1, serves as the ligand for EDAR. EDA-A2, which differs from EDA-A1 by the deletion of two amino acids, binds only the X-linked ectodysplasin-A2 receptor (XEDAR). Both EDAR and XEDAR exhibit homology with TROY.

Function:
Receptor for EDA isoform A1, but not for EDA isoform A2. Mediates the activation of NF-kappa-B and JNK. May promote caspase-independent cell death.

Subunit:
Binds to EDARADD. Associates with TRAF1, TRAF2, TRAF3 and NIK.

Subcellular Location:
Membrane; Single-pass type I membrane protein (Probable).

Tissue Specificity:
Detected in fetal kidney, lung, skin and cultured neonatal epidermal keratinocytes. Not detected in lymphoblast and fibroblast cell lines.

DISEASE:
Defects in EDAR are a cause of ectodermal dysplasia anhidrotic (EDA) [MIM:224900]; also known ectodermal dysplasia hypohidrotic autosomal recessive (HED). Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EDA is characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. Defects in EDAR are the cause of ectodermal dysplasia type 3 (ED3) [MIM:129490]; also known as ectodermal dysplasia hypohidrotic autosomal dominant or EDA3. ED3 is an autosomal dominant condition characterized by hypotrichosis, abnormal or missing teeth, and hypohidrosis due to the absence of sweat glands.

Similarity:
Contains 1 death domain.
Contains 3 TNFR-Cys repeats.

Database links:

Entrez Gene: 10913 Human

Entrez Gene: 13608 Mouse

Entrez Gene: 365581 Rat

Omim: 604095 Human

SwissProt: Q9UNE0 Human

SwissProt: Q9R187 Mouse

Unigene: 171971 Human

Unigene: 174523 Mouse

Unigene: 133578 Rat



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.rvdoil.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
国产91精品秘 入福利姬 | 我把黑丝美女操喷水内射视频 | 影音先锋中文字幕在线观看 | 少妇人妻偷人精品视频蜜桃 | 狠狠躁91人妻二三区 | 久久久久久久久久久久久久动漫 | 精品国产精品无码A片久久妖精 | 亚洲高清国产传媒免费视频 | 国产寡妇婬乱A毛片视频图片 | 国产无码高清视频日韩 | 国产又粗又猛又爽视频 | 国产亲子乱婬一级A片 | 国产黃色A片三級三級三級四川 | 亚洲BBBB爽爽爽自慰 | 亚洲无码在线观看视频 | www.com黄色的网站污在线观看 | 国产欧美在线观看不卡高清 | 国产91足控脚交在线 | 欧美视频一区二区三区 | 久久久久久九九99精品 | 精品少妇人妻av无码中文字幕 | 日日夜夜爱爱鲁鲁舔舔 | 久久久久久91香蕉国产 | 一区二区三区久久 | 按摩一级婬乱片A片 | 黄色一级片永久免费看 | 四虎884aa成人精品 | 91大神大课约女教师在线观看 | 丰满熟女人妻中出系列 | 一级毛片生活黄色的 | 日本久久无码精品一级A片直播 | 蜜臀久久精品久久久久消防站 | 寡妇高潮一级毛片免费看大胸 | 四季亚洲AV无码一区二区三匹在线观看 | 淫淫色色麻豆传媒 | 亚洲无码乱码精品国产 | 少女免费观看片哔哩哔哩在线观看视频 | 国产91亚洲精品成人AA片p站 | 国产丝袜视频在线观看 | 日韩AV免费在线观看网站 | 四川少妇搡BBBBB搡BBB |