Detectionof Thrombomodulin/BDCA‑3 in Human PBMCs by Flow Cytometry.
Human peripheral blood mononuclearcells (PBMCs) were stained with Mouse Anti-Human Thrombomodulin/BDCA‑3PE‑conjugated Monoclonal Antibody (Catalog # FAB3947P) and MouseAnti-Human HLA‑DR APC‑conjugated Monoclonal Antibody(Catalog # FAB4869A).Quadrant markers were set based on internal control antibody staining. View ourprotocol for StainingMembrane-associated Proteins.
Preparation and Storage
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Protect from light. Do not freeze.
12 months from date of receipt, 2 to 8 °C as supplied.
Encoded by the THBD gene, Thrombomodulin is also known as Blood Dendritic Cell Antigen 3 (BDCA‑3) and designated CD141. The deduced amino acid (aa) sequence of human THBD predicts a signal peptide (aa 1‑18) and a mature chain (aa 19‑575) that consists of the following domains: C‑type lectin (aa 31‑169), EGF‑like (aa 241‑281, aa 284‑324, aa 325‑363, aa 365‑405, aa 404‑440, and aa 441‑481), transmembrane (aa 516 to 539) and cytoplasmic (aa 540‑575). The region used as an immunogen consists of aa 19‑515, corresponding to the extracellular portion of the type I membrane protein. Predominantly synthesized by vascular endothelial cells, THBD inhibits coagulation and fibrinolysis (1‑3). It functions as a cell surface receptor and an essential cofactor for active Thrombin, which in turn activates protein C and Thrombin‑Activatable Fibrinolysis Inhibitor (TAFI), also known as Carboxypeptidase B2 (CPB2). Activated Protein C (APC), facilitated by Protein S, degrades coagulation factors Va and VIIIa, which are required for Thrombin activation. Activated CPB2 cleaves basic C‑terminal aa residues of its substrates, including Fibrin, preventing the conversion of Plasminogen to Plasmin. In addition, THBD gene polymorphisims are associated with human disease and THBD plays a role in thrombosis, stroke, arteriosclerosis, and cancer (4). For example, increased serum levels of THBD, due to protease cleavage, have been associated with smoking, cardiac surgery, atherosclerosis, liver cirrhosis, diabetes mellitus, cerebral and myocardial infarction, and multiple sclerosis (5).
Van de Wouwer, M. et al. (2004) Arterioscler. Thromb. Vasc. 24:1374.
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