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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 | Narlumosbart Biosimilar - Anti-ODF mAb - Research Grade |
|---|---|
| Species | Homo sapiens |
| Expression system | XtenCHO |
| Purity | >90% by SDS-PAGE. |
| Buffer | 0.01M PBS, pH 7.4. |
| Delivery condition | Blue ice (+4°C) |
| Delivery Time | 3-5 days if in stock; 3-5 weeks if production needed |
| Storage condition | 4°C for short term; -20°C for long term |
| Brand | ProteoGenix |
| Aliases /Synonyms | anti-ODF, TNF-related activation-induced cytokine, Osteoclast differentiation factor, TNFSF11, TRANCE, Osteoprotegerin ligand, RANKL, Tumor necrosis factor ligand superfamily member 11, Receptor activator of nuclear factor kappa-B ligand, CD254, OPGL |
| Reference | PX-TA2079 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG4-kappa |
| Clonality | Monoclonal Antibody |
Narlumosbart Biosimilar – Anti-ODF mAb – Research Grade: A Revolutionary Antibody for Targeting ODF
Narlumosbart Biosimilar – Anti-ODF mAb – Research Grade is a highly specialized antibody that has been developed for targeting ODF (osteoclast differentiation factor). This biosimilar is a groundbreaking advancement in the field of therapeutic antibodies and has the potential to revolutionize the treatment of diseases associated with ODF.
Narlumosbart Biosimilar is a monoclonal antibody (mAb) that is produced by recombinant DNA technology. It is a biosimilar of the well-known anti-ODF mAb, denosumab. The structure of Narlumosbart Biosimilar is very similar to denosumab, with only minor differences in the amino acid sequence. This makes it highly specific and effective in targeting ODF.
Narlumosbart Biosimilar works by binding to ODF and preventing its interaction with its receptor, RANK (receptor activator of nuclear factor kappa-B). This inhibits the activation of osteoclasts, which are responsible for bone resorption. By blocking ODF, Narlumosbart Biosimilar helps in maintaining bone density and preventing bone loss in diseases such as osteoporosis and bone metastases.
In addition to its activity against ODF, Narlumosbart Biosimilar also has anti-inflammatory properties. It has been shown to reduce the production of inflammatory cytokines, such as TNF-alpha and IL-6, which are involved in the pathogenesis of various inflammatory diseases.
Narlumosbart Biosimilar has a wide range of potential applications in the field of medicine. Its primary use is in the treatment of diseases associated with ODF, such as osteoporosis, bone metastases, and Paget’s disease. It can also be used in the management of other bone-related disorders, such as multiple myeloma and giant cell tumor of bone.
Furthermore, Narlumosbart Biosimilar has shown promising results in the treatment of inflammatory conditions, such as rheumatoid arthritis and psoriatic arthritis. Its anti-inflammatory properties make it a potential candidate for the management of these diseases, which are characterized by excessive bone destruction and inflammation.
Narlumosbart Biosimilar is currently in the research phase and is not yet available for clinical use. However, the results of preclinical studies have been very promising, and it is expected to enter clinical trials soon. This research grade biosimilar is being developed by a team of highly experienced scientists and researchers, who are dedicated to bringing this revolutionary antibody to the market.
Narlumosbart Biosimilar – Anti-ODF mAb – Research Grade is a highly specialized antibody that has the potential to transform the treatment of diseases associated with ODF. Its structure, activity, and potential applications make it a promising candidate for the management of bone-related disorders and inflammatory conditions. As it progresses through clinical trials, Narlumosbart Biosimilar has the potential to become a game-changer in the field of therapeutic antibodies.
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