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  人才招聘  關于我們  聯(lián)系我們
欧美日本精品一区二区三区,欧美日韩精品久久久免费观看5分钟
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Thrombomodulin/BF555 Conjugated antibody (bs-20395R-BF555)
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-20395R-BF555
英文名稱1 Rabbit Anti-Thrombomodulin/BF555 Conjugated antibody
中文名稱 BF555標記的血栓調節(jié)蛋白抗體
別    名 Thrombomodulin; CD 141; CD141; CD141 antigen; Fetomodulin; THBD; THRM; TM; AHUS 6; AHUS6; BDCA 3; BDCA3; THPH12; TRBM_HUMAN.  
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  神經生物學  血管內皮細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse,  (predicted: Dog, Cow, Sheep, )
產品應用 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 61kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Thrombomodulin
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.
產品介紹 background:
Thrombomodulin, TM is cell surface glycoprotein; plays an important role in the protein C anticoagulant pathway. It located in a vein, artery and capillary endothelial cells on the surface of plasma membrane protein. It is generally believed: TM vascular endothelial injury is an important parameter is the thrombin receptor, known in a variety of normal human tissues, can also be expressed in many tumors, TM may be similar to the E-cadherin,and is a lectin Like activity of a new class of members of the cell adhesion molecules.
CD141/Thrombomodulin is an exclusively endothelial cell surface glycoprotein that forms a 1:1 complex with thrombin. Binding of thrombin to this high-affinity receptor alters its specificity toward several substrates. The complex activates protein C approximately 1000 times faster than thrombin alone. Activated protein C degrades clotting factors V and VIII; thus, thrombomodulin converts thrombin into a physiologic anticoagulant. Thrombomodulin is also found in the circulatory and urinary systems, the physiologic significance of this is obscure.

Function:
Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated.

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

Tissue Specificity:
Endothelial cells are unique in synthesizing thrombomodulin.

Post-translational modifications:
N-glycosylated.
The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains.

DISEASE:
Defects in THBD are the cause of thrombophilia due to thrombomodulin defect (THPH12) [MIM:614486]. A hemostatic disorder characterized by a tendency to thrombosis.
Defects in THBD are a cause of susceptibility to hemolytic uremic syndrome atypical type 6 (AHUS6) [MIM:612926]. An atypical form of hemolytic uremic syndrome. It is a complex genetic disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, renal failure and absence of episodes of enterocolitis and diarrhea. In contrast to typical hemolytic uremic syndrome, atypical forms have a poorer prognosis, with higher death rates and frequent progression to end-stage renal disease. Note=Susceptibility to the development of atypical hemolytic uremic syndrome can be conferred by mutations in various components of or regulatory factors in the complement cascade system. Other genes may play a role in modifying the phenotype.

Similarity:
Contains 1 C-type lectin domain.
Contains 6 EGF-like domains.

Database links:

Entrez Gene: 7056 Human

Omim: 188040 Human

SwissProt: P07204 Human

Unigene: 2030 Human



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

血栓調節(jié)蛋白(thrombomodulin,TM)是一種分布于靜脈、動脈和毛細血管內皮細胞表面的質膜蛋白。 一般認為:TM是血管內皮損傷的重要參數,也是凝血酶的受體,已知在人類多種正常組織中表達,亦可表達于許多腫瘤組織,TM可能類似于鈣粘蛋白,是具有凝集素樣活性的新一類細胞粘附分子的成員。TM是血管內皮細胞膜上的凝血酶受體之一。與凝血酶結合后可降低凝血酶的凝血活性,而加強其激活蛋白C的活性。由于被激活的蛋白C具有抗凝作用,因此,TM是使凝血酶由促凝轉向抗凝的重要的血管內凝血抑制因子。
版權所有 2004-2026 www.m.p2b3.cn 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         京公網安備110107000727號
欧美日韩一区二区在线不卡| 亚洲线日本一区二区三区| 国产乱老熟女乱老熟女视频| 国产精品国语对白在线观看| 久久精一区二区三区| 久久婷婷综合激情亚洲狠狠| 久久精品国产亚洲高清| 日韩欧美精品在线中文字幕| 亚洲不卡一区二区三区在线| 欧美日韩一区二区中文字幕| 亚洲欧美成人激情在线| 狠狠色噜噜狠狠亚洲AV| 亚洲人妻一区二区久久| 色欲aⅴ亚洲情无码AV蜜桃| 日韩一二三区中文字幕在线视频精品| 一区二区三区精品亚洲视频| 国产A级三级三级三级视频| 久久国产成人高清精品亚洲| 韩国三级电影视频网站| 亚州在线中文字幕经典a| 婷婷色婷婷开心五月四房播播| 精品国产尤物久久久久久| 国产精品23一区二区| 韩国午夜理伦三级理论电影| 国产精品一区二区久久hs| 亚洲国产午夜精品不卡| 欧美日韩成人精品久久久| 久久精品亚洲成在人线av| 精品国产日本一区二区| 一区二区三区四区欧美日韩亚洲| 亚洲精品国自产在线| 欧美日韩专区一区二区| 国产综合精品久久久久成人蜜臀| 久久秘一区二区三区| 久久久高清免费精品视频| 久久久久成人精品免费播放寂寞少妇| 亚洲欧洲日韩综合网站| 亚洲精品日韩在线丰满| 亚洲国产午夜精品不卡| 黄色网色网色网色网色网站| 97在线视频播放免费观看不卡|