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Native Human Carcinoembryonic Antigen was purified from Human Liver Metastases.Members of the CEACAM subfamily, including CEACAM5, belong to the CEA gene family. For general information on the CEA gene family, see CEACAM1.
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PLAU or urokinase-type plasminogen activator (uPA) critically initiates fibrinolysis by cleaving plasminogen to form active plasmin This enzymatic conversion is critical for regulating clot dissolution and tissue remodeling PLAU/uPA Protein Mouse (Biotinylated HEK293 His-Avi) is the recombinant mouse-derived PLAU/uPA protein expressed by HEK293 with C-Avi C-His labeled tag
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
PLAU or urokinase-type plasminogen activator (uPA) critically initiates fibrinolysis by cleaving plasminogen to form active plasmin This enzymatic conversion is critical for regulating clot dissolution and tissue remodeling PLAU/uPA Protein Mouse (HEK293 C-His-Avi) is the recombinant mouse-derived PLAU/uPA protein expressed by HEK293 with C-His-Avi labeled tag
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MW 1666.16 g/mol. Toll-like receptor 2/6 (TLR2/6) agonist. Synthetic lipoprotein. Represents N-terminal part of Mycoplasma salivarium LP44. NF-κB and MAPK pathway activator. Active in vivo. Rstereoisomer of FSL-1 (ab144863).
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The DPP4 gene encodes dipeptidyl peptidase 4 which is identical to adenosine deaminase complexing protein-2 and to the T-cell activation antigen CD26 It is an intrinsic type II transmembrane glycoprotein and a serine exopeptidase that cleaves X-proline dipeptides from the N-terminus of polypeptides Dipeptidyl peptidase 4 is highly involved in glucose and insulin metabolism as well as in immune regulation This protein was shown to be a functional receptor for Middle East respiratory syndrome coronavirus (MERS-CoV) and protein modeling suggests that it may play a similar role with SARS-CoV-2 the virus responsible for COVID-19
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An inhibitor of cardiac myosin ATPase (IC50 1.26 UM for the bovine enzyme) reduces fractional shortening in isolated rat cardiac ventricular myocytes (IC50 7.9 UM) as well as in rats in a dose-dependent manner
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MW 560.64 g/mol, Purity >98%. Selective Hsp90 inhibitor. Binds the ATP site of Hsp90 and inhibits chaperone activity. A benzoquinone ansamycin antibiotic. Also inhibits the Hsp90 paralog GRP94. Exhibits various cellular actions including gene expression, cell proliferation, apoptosis and angiogenesis.
Lipoprotein Lipase (LPL) is majorly secreted by myocytes and adipocytes in humans and is crucial for triglyceride homeostatis. Mutations in the catalytic domain of LPL impairs its interaction with glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 (GPIHBP1). The N-terminal catalytic domain is essential for lipolysis. The C-terminal is crucial for binding lipoproteins. Altered LPL levels may play role in the pathogenesis of atherosclerosis coronary heart disease and chronic lymphocytic leukemia.
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