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(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
国产一区二区不卡,国产做受91 一片二
Rabbit Anti-CD105/PE Conjugated antibody (bs-4609R-PE)
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(jià)
產(chǎn)品編號(hào) bs-4609R-PE
英文名稱 Rabbit Anti-CD105/PE Conjugated antibody
中文名稱 PE標(biāo)記的內(nèi)皮糖蛋白抗體
別    名 END; Endoglin; ENG; FLJ41744; HHT1; ORW; ORW1; Osler Rendu Weber syndrome 1; RP11 228B15.2; CD 105; CD105 antigen; EGLN_HUMAN; AI528660; AI662476; S-endoglin; SN6.  
Journal
PMID
IF
Application
[IF=5.47] Gao, Xin, et al. "Identification of Rat Respiratory Mucosa Stem Cells and Comparison of the Early Neural Differentiation Potential with the Bone Marrow Mesenchymal Stem Cells In Vitro." Cellular and Molecular Neurobiology: 1-12.  FCM ;  Rat.  
[IF=2.51] Gao, Xin, et al. "Identification of rat respiratory Mucosa stem cells and comparison of the early neural differentiation potential with the bone marrow mesenchymal stem cells in vitro." Cellular and molecular neurobiology 34.2 (2014): 257-268  FCM ;  Rat.  
[IF=2.2] Gierloff, M., et al. "In vitro comparison of different carrier materials with rat bone marrow MSCs." Clinical Oral Investigations (2013): 1-13.  Rat.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 腫瘤  心血管  細(xì)胞生物  免疫學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  干細(xì)胞  細(xì)胞膜受體  細(xì)胞表面分子  血管內(nèi)皮細(xì)胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, )
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 70kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CD105/Endoglin
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 homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

Function:
Major glycoprotein of vascular endothelium. May play a critical role in the binding of endothelial cells to integrins and/or other RGD receptors.

Subunit:
Homodimer that forms an heteromeric complex with the signaling receptors for transforming growth factor-beta: TGFBR1 and/or TGFBR2. It is able to bind TGF-beta 1, and 3 efficiently and TGF-beta 2 less efficiently. Interacts with TCTEX1D4. Interacts with ARRB2.

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

Tissue Specificity:
Endoglin is restricted to endothelial cells in all tissues except bone marrow.

DISEASE:
Defects in ENG are the cause of hereditary hemorrhagic telangiectasia type 1 (HHT1) [MIM:187300]; also known as Osler-Rendu-Weber syndrome 1 (ORW1). HHT1 is an autosomal dominant multisystemic vascular dysplasia, characterized by recurrent epistaxis, muco-cutaneous telangiectases, gastro-intestinal hemorrhage, and pulmonary (PAVM), cerebral (CAVM) and hepatic arteriovenous malformations; all secondary manifestations of the underlying vascular dysplasia. Although the first symptom of HHT1 in children is generally nose bleed, there is an important clinical heterogeneity.

Database links:

Entrez Gene: 2022 Human

Entrez Gene: 13805 Mouse

Entrez Gene: 497010 Rat

Omim: 131195 Human

SwissProt: P17813 Human

SwissProt: Q63961 Mouse

Unigene: 76753 Human

Unigene: 225297 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.nmgps.com 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(hào): 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(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
水蜜桃AV无码专区亚洲AV麻豆 | 婷婷色情乱婬一区二区三区小说 | 性感成熟动漫美女在线观看一区二区的 | 寡妇一夜被躁高潮A片小 | 亚洲国产精品综合久久99视频 | 深圳妇女搡BBBB搡BBBB | 女教师一级特黄大片630 | 午夜福利一区二区三区 | 国产一级a毛一级a看… | 国产精品偷乱一区二区三区 | 国产无码在线观看网站27 | 国产成人无码A片V99 | 婷婷99狠狠躁天天躁中文字幕 | 蜜桃视频一区二区三区 | 亚洲黄色免费在线视频 | 亚洲AV成人一区二区三区观看 | 中文字幕亚洲乱码熟女在线萌芽 | 又紧又大又硬又粗视频 | 日韩精品在线播放 | 91 国产在线播放竹菊 | 特级婬片A片AAA毛片A级面粉 | 国产免费色情网站入口大全 | 人人肉人人操人人爽 | 婷婷五月天一区二区 | 99人妻字幕乱码久久99一三区 | 国产91无码精品秘 入口、 | 国产99久久久久久久久 | 精品人妻伦一二三区久久尼寺 | 91清纯白嫩初高中在线 | 国产 刺激 高潮 免 国产毛片AAAAA级 | 中文字幕一区二区人妻久久 | 一区少妇白洁无码视频 | 一级二级三级资源在线观看 | 强伦轩一级A片免费播放 | 亚洲久久久成人网站 | 国产无遮挡无黄又爽农村妇女 | 少妇激情一区二区三区久久大香香 | 四川大BBB搡BBB搡视频 | 国产精品无码久久久久一区二区 | 波多野结衣av一区二区蜜桃观看 | 91蜜桃传媒麻豆中文字幕 |