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Lerodalcibep (LIB003) is a potent, high-affinity inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9). It is a recombinant fusion protein comprising a small PCSK9-binding protein fused to human serum albumin (HSA) to significantly extend its circulatory half-life. Lerodalcibep binds to circulating PCSK9 and blocks its interaction with low-density lipoprotein receptors (LDLR) on the hepatocyte surface, preventing lysosomal degradation of the receptors. This mechanism increases the density of LDLR on the liver surface, leading to the highly efficient clearance of LDL-cholesterol (LDL-C) from the blood.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | Inquiry | 4-6 weeks | 4-6 weeks | |
| 50 mg | Inquiry | 4-6 weeks | 4-6 weeks |
| Description | Lerodalcibep (LIB003) is a potent, high-affinity inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9). It is a recombinant fusion protein comprising a small PCSK9-binding protein fused to human serum albumin (HSA) to significantly extend its circulatory half-life. Lerodalcibep binds to circulating PCSK9 and blocks its interaction with low-density lipoprotein receptors (LDLR) on the hepatocyte surface, preventing lysosomal degradation of the receptors. This mechanism increases the density of LDLR on the liver surface, leading to the highly efficient clearance of LDL-cholesterol (LDL-C) from the blood. |
| Synonyms | LIB003 |
| Reactivity | Human |
| Application | FACS Functional assay |
| Antibody Type | Monoclonal |
| Formulation | Supplied as a sterile solution in a buffered formulation system (e.g., phosphate-, citrate-, or amino acid-based). Please refer to the CoA for lot-specific composition. |
| Endotoxin | <1.0 EU/mg |
| Conjucates | Unconjugated |
| Target | PCSK9 |
| Cas No. | 2250073-78-8 |
| Storage | store at low temperature | store at -20°C | Shipping with blue ice/Shipping at ambient temperature. |
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