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| Size | 100µg, 1MG |
|---|---|
| Isotype | IgG1, lambda |
| Brand | ProteoGenix |
| Product type | Primary Antibodies |
| Clonality | Monoclonal Antibody |
| Expression system | XtenCHO |
| Applications | Elisa, WB |
| Product name | Bintrafusp Biosimilar - Anti-CD274 mAb - Research Grade |
|---|---|
| Species | Fusion |
| 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 | Bintrafusp,,CD274,anti-CD274 |
| Reference | PX-TA1819 |
| Note | For research use only. Not suitable for clinical or therapeutic use. |
| Isotype | IgG1 Lambda |
| Clonality | Monoclonal Antibody |
Bintrafusp Biosimilar: A Revolutionary Anti-CD274 mAb
Bintrafusp Biosimilar, also known as anti-CD274 mAb, is a monoclonal antibody that has been developed as a promising therapeutic agent for various diseases. This biosimilar is a highly specific and potent inhibitor of the immune checkpoint protein CD274, also known as programmed death-ligand 1 (PD-L1). Its unique structure and mechanism of action make it a promising candidate for the treatment of various cancers and autoimmune disorders.
Bintrafusp Biosimilar is a fusion protein composed of two different components: a monoclonal antibody and a TGF-β receptor II (TGF-βRII) fusion protein. The monoclonal antibody component is a fully human IgG1 antibody that binds to the extracellular domain of CD274 with high affinity. This results in the blockade of the PD-L1/PD-1 signaling pathway, which is crucial for the suppression of immune responses in cancer and autoimmune diseases.
The TGF-βRII fusion protein component of Bintrafusp Biosimilar is a modified form of the TGF-β receptor II, which is a key regulator of the TGF-β signaling pathway. This component acts as a “trap” for TGF-β, preventing it from binding to its receptors and inhibiting TGF-β signaling. This dual mechanism of action of Bintrafusp Biosimilar, targeting both PD-L1 and TGF-β, makes it a potent inhibitor of tumor growth and immune suppression.
Bintrafusp Biosimilar has been extensively studied in preclinical and clinical trials, and its activity has been demonstrated in various cancer types and autoimmune diseases. In cancer, Bintrafusp Biosimilar has shown promising results in inhibiting tumor growth and metastasis, as well as enhancing anti-tumor immune responses. It has also shown potential in overcoming resistance to other cancer therapies, such as immune checkpoint inhibitors.
In autoimmune diseases, Bintrafusp Biosimilar has shown efficacy in preclinical models of rheumatoid arthritis, lupus, and multiple sclerosis. Its ability to block the TGF-β signaling pathway, which is involved in the pathogenesis of these diseases, makes it a promising therapeutic option for patients with these conditions.
Bintrafusp Biosimilar is currently being evaluated in clinical trials for the treatment of various cancers, including non-small cell lung cancer, head and neck cancer, and cervical cancer. It is also being studied in combination with other therapies, such as chemotherapy and immune checkpoint inhibitors, to assess its potential in improving patient outcomes.
In addition, Bintrafusp Biosimilar is being investigated for the treatment of autoimmune diseases, with a focus on rheumatoid arthritis and lupus. These trials aim to evaluate the safety and efficacy of this biosimilar in patients with these conditions, and to determine the optimal dosing and treatment regimens.
Bintrafusp Biosimilar is a promising therapeutic agent with a unique structure and dual mechanism of action. Its ability to target both PD-L1 and TGF-β makes it a potent inhibitor of tumor growth and immune suppression, and it has shown promising results in preclinical and clinical studies. With ongoing research and development, Bintrafusp Biosimilar has the potential to become a game-changing treatment option for patients with cancer and autoimmune diseases.
Bintrafusp Biosimilar, anti-CD274 mAb, monoclonal antibody, TGF-β receptor II, immune checkpoint, PD-L1, tumor growth, autoimmune diseases, cancer, clinical trials, therapeutic agent.
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