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| Size | 100ug, 1MG |
|---|---|
| Isotype | IgG4, kappa |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Mibavademab Biosimilar - Anti-LEPR mAb - Research Grade |
|---|---|
| Source | CAS 2305770-44-7 |
| Species | Humanized |
| Purity | >85% |
| Buffer | PBS buffer PH7.5 |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3 week if production needed |
| Storage condition | store at -80°C |
| Brand | ProteoGenix |
| Aliases /Synonyms | Mibavademab,IMMUNOGLOBULIN G4 (227-PROLINE), ANTI-(HUMAN LEPTIN RECEPTOR) (HUMAN MONOCLONAL REGN4461 .GAMMA.4-CHAIN), DISULFIDE WITH HUMAN MONOCLONAL REGN4461 .KAPPA.-CHAIN, DIMER, REGN4461, REGN-4461,LEPR,anti-LEPR |
| Reference | PX-TA1684 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4,Kappa |
| Clonality | Monoclonal Antibody |
Mibavademab Biosimilar, also known as Anti-LEPR mAb, is a monoclonal antibody that targets the Leptin Receptor (LEPR). It is a biosimilar version of the original Mibavademab, which is a fully humanized anti-LEPR monoclonal antibody. The structure of Mibavademab Biosimilar is similar to that of its originator, with a few minor differences.
Mibavademab Biosimilar is composed of two identical heavy chains and two identical light chains, each consisting of a variable region and a constant region. The variable regions of the heavy and light chains are responsible for binding to the LEPR receptor, while the constant regions provide stability and effector functions.
The variable region of Mibavademab Biosimilar is made up of six complementarity-determining regions (CDRs), which are responsible for the antibody’s specificity and affinity towards the LEPR receptor. These CDRs are located at the tip of the antibody’s “Y” shape and interact with specific amino acids on the LEPR receptor to form a strong bond.
Mibavademab Biosimilar is a potent inhibitor of the LEPR receptor, which is a key regulator of energy balance and metabolism. The binding of Mibavademab Biosimilar to the LEPR receptor prevents the binding of leptin, the hormone responsible for signaling satiety, thereby inhibiting its activity.
This inhibition of the LEPR receptor leads to a decrease in food intake and an increase in energy expenditure, making Mibavademab Biosimilar a potential treatment for obesity and related metabolic disorders. In addition, Mibavademab Biosimilar has also shown potential in regulating glucose and lipid metabolism, making it a promising therapeutic option for type 2 diabetes and dyslipidemia.
Mibavademab Biosimilar is currently being developed as a research-grade antibody for preclinical studies and clinical trials. It has shown promising results in animal models, demonstrating its potential as a therapeutic option for obesity and metabolic disorders.
In addition to its potential in treating obesity and related metabolic disorders, Mibavademab Biosimilar has also shown potential in other areas of research. It has been studied for its role in regulating immune responses and its potential in treating autoimmune diseases such as multiple sclerosis and rheumatoid arthritis.
Mibavademab Biosimilar is also being explored as a potential treatment for certain types of cancer. The LEPR receptor has been found to be overexpressed in certain types of cancer, and by targeting this receptor, Mibavademab Biosimilar may have anti-tumor effects.
In conclusion, Mibavademab Biosimilar – Anti-LEPR mAb is a promising antibody with potential applications in the treatment of obesity, metabolic disorders, autoimmune diseases, and cancer. Its specific structure and activity make it a valuable tool for research and a potential therapeutic option for various diseases. Further studies and clinical trials are needed to fully understand the potential of Mibavademab Biosimilar and its role in improving human health.
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