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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | Mammalian cells |
| Applications | Elisa, WB |
| Product name | Frovocimab Biosimilar - Anti-PCSK9 mAb - Research Grade |
|---|---|
| Source | CAS 1643672-70-1 |
| Species | Humanized |
| Expression system | Mammalian cells |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Frovocimab,LY-3015014,PCSK9,anti-PCSK9 |
| Reference | PX-TA1527 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Frovocimab Biosimilar, also known as Anti-PCSK9 mAb, is a research grade antibody that has shown promising results in the treatment of various diseases. This article will provide a comprehensive description of the structure, activity, and potential applications of this novel therapeutic target.
Frovocimab Biosimilar is a monoclonal antibody (mAb) that specifically targets PCSK9 (proprotein convertase subtilisin/kexin type 9), a protein involved in the regulation of cholesterol levels in the body. It is a fully humanized IgG1 antibody, meaning it is derived from human genes and has a similar structure to natural antibodies produced by the body.
The antibody consists of two heavy chains and two light chains, connected by disulfide bonds. The variable regions of the antibody, responsible for binding to PCSK9, are located at the tips of the heavy and light chains. This unique structure allows the antibody to specifically bind to PCSK9 and inhibit its activity.
Frovocimab Biosimilar works by blocking the interaction between PCSK9 and the LDL receptor (LDLR). PCSK9 normally binds to the LDLR and targets it for degradation, leading to increased levels of LDL cholesterol in the blood. By inhibiting this interaction, Frovocimab Biosimilar increases the number of LDLRs on the surface of cells, resulting in increased clearance of LDL cholesterol from the blood.
In addition, Frovocimab Biosimilar has been shown to reduce the production of PCSK9 by liver cells, further decreasing the levels of LDL cholesterol in the blood. This dual mechanism of action makes Frovocimab Biosimilar a highly effective therapeutic target for lowering LDL cholesterol levels.
Frovocimab Biosimilar has shown promising results in the treatment of various diseases related to high levels of LDL cholesterol, including familial hypercholesterolemia and atherosclerosis. It has also been studied as a potential treatment for other conditions such as non-alcoholic fatty liver disease and type 2 diabetes.
In addition, Frovocimab Biosimilar has the potential to be used in combination with other lipid-lowering therapies, such as statins, to further reduce LDL cholesterol levels. This makes it a valuable addition to the current treatment options for patients with high cholesterol levels.
In summary, Frovocimab Biosimilar is a promising therapeutic target for the treatment of diseases related to high levels of LDL cholesterol. Its unique structure and dual mechanism of action make it a highly effective antibody for inhibiting the activity of PCSK9 and lowering LDL cholesterol levels. Further research and clinical trials are needed to fully explore the potential applications of this novel antibody in the treatment of various diseases.
Immobilized Human PCSK9 recombinant protein (cat. No.PX-P5124) at 0.5µg/mL (100µL/well) can bind to Frovocimab Biosimilar - Anti-PCSK9 mAb (cat. No.PX-TA1527) in indirect ELISA with Goat Anti-Human IgG secondary antibody coupled with HRP measured by OD450
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