Rabbit Anti-Thrombomodulin antibody |
反应物种(预测) |
Human,Mouse,Rat,Dog,Cow |
产品应用(可尝试) |
WB,ICC,IF,ELISA |
推荐稀释比例 |
WB=1:500-2000,Elisa=1:5000-10000,IF=1:100-500,ICC=1:100-500, |
研究领域 |
心血管,转运蛋白,糖蛋白,内皮细胞, |
标签 |
Array |
RRID:AB_10856058
产品名称:Rabbit Anti-Thrombomodulin antibody
别名: CD 141; CD141; CD141 antigen; Fetomodulin; THBD; THRM; TM; AHUS 6; AHUS6; BDCA 3; BDCA3; THPH12; TRBM_HUMAN.
中文名称:凝血调节蛋白/血栓调节素抗体
英文名称:Rabbit Anti-Thrombomodulin antibody
抗体来源: Rabbit
克隆类型:多克隆
细胞定位:细胞膜
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein A
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
免 疫 原:KLH conjugated synthetic peptide derived from human CD141
抗原表位:81-180/575
SWISS:P07204
Gene ID :7056
Human Gene ID:7056
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 activ
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 typ
Similarity:Contains 1 C-type lectin domain.
Contains 6 EGF-like domains.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.