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Sino Biological Inc. liefert Rat Thrombomodulin / THBD Protein (His Tag) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.
Weitere Informationen über Rat Thrombomodulin / THBD Protein (His Tag) lesen Sie bitte: http://www.sinobiological.com/Thrombomodulin-THBD-Protein-g-10329.html
| Synonym | THBD |
| Protein Construction | A DNA sequence encoding the rat THBD(O35370) (Met1-Ser517) was expressed with a polyhistidine tag at the C-terminus. |
| Source | Rat |
| Expression Host | Human Cells |
| Purity | > 90 % as determined by SDS-PAGE | SDS-PAGE:![]() THBD protein |
| Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method | |
| Stability | Samples are stable for up to twelve months from date of receipt at -70℃ | |
| Predicted N terminal | Ile 17 | |
| Molecular Mass | The recombinant rat THBD comprises 512 amino acids and predicts a molecular mass of 55.2 kDa. The apparent molecular mass of the recombinant protein is approximately 95 kDa in SDS-PAGE under reducing conditions due to glycosylation. | |
| Formulation | Lyophilized from sterile PBS, pH 7.4.
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| Storage | Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles. |
| Reconstitution | A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information. |
Thrombomodulin, also known as THBD(CD141), is an integral membrane protein which expressed on the surface of endothelial cells and serves as a cofactor for thrombin. It is also expressed on human mesothelial cell, monocyte and a dendritic cell subset. Thrombomodulin reduces blood coagulation by converting thrombin to an anticoagulant enzyme from a procoagulant enzyme. Thrombomodulin functions as a cofactor in the thrombin-induced activation of protein C in the anticoagulant pathway by forming a 1:1 stoichiometric complex with thrombin. Thrombomodulin also regulates C3b inactivation by factor I. Mutations in the thrombomodulin gene have also been reported to be associated with atypical hemolytic-uremic syndrome.